Professional Documents
Culture Documents
Galapagos Manual
Galapagos Manual
Version 1.1.2.0
Contents
Contents ............................................................................................................. 2
EZ Read Microplate Reader Health and Safety Information.............................. 5
Software Licence Agreement..............................................................................17
How to get Help ................................................................................................19
Display 'About' Information................................................................................22
Contact Biochrom Limited ..................................................................................24
User Interface Overview .................................................................................. 25
Starting the Application .....................................................................................27
Application Ribbons ...........................................................................................27
Data Window Overview......................................................................................30
Exiting the Application .......................................................................................35
Data Management ............................................................................................ 37
New .................................................................................................................38
Open................................................................................................................39
Save As............................................................................................................42
Database Connection and Management ..............................................................45
Import .............................................................................................................56
Export ..............................................................................................................57
Export Options..................................................................................................61
Print and Print Preview ......................................................................................65
Copy ................................................................................................................67
Recent .............................................................................................................68
Data Validity..................................................................................................... 69
Instrument Management ................................................................................. 70
Connecting to an Instrument .............................................................................70
EZ Read Models ................................................................................................75
Instrument Window .......................................................................................76
Instrument Properties: General ...................................................................78
Instrument Properties: Methods and Plate Data ............................................82
Instrument Properties: Plate Definitions .......................................................89
Instrument Properties: Transport.................................................................91
Instrument Properties: Wavelength Calibration .............................................92
Anthos Models ..................................................................................................96
Instrument Window .......................................................................................96
Instrument Properties: General ...................................................................98
ASYS Models................................................................................................... 100
Page 2 of 381
Instrument Window ..................................................................................... 100
Instrument Properties: General ................................................................. 103
Instrument Properties: Methods and Plate Data .......................................... 108
Instrument Properties: Plate Definitions ..................................................... 115
Instrument Properties: Transport............................................................... 117
Instrument Properties: Wavelength Calibration ........................................... 118
Methods .......................................................................................................... 122
Quick Measurement ........................................................................................ 123
Acquiring Using Quick Measurement ................................................................. 124
Changing the Plate Layout ............................................................................... 155
Saving a Method Template .............................................................................. 176
Opening a Method Template ............................................................................ 178
Plate Tools...................................................................................................... 180
Plate Definition Editor ...................................................................................... 180
Saving and Opening Plate Definitions ............................................................... 182
Creating Plate Definitions ................................................................................ 189
Removing Plate Definitions from the Database .................................................. 194
Plate Layout Editor .......................................................................................... 196
Saving and Opening Plate Layouts.................................................................... 204
Creating and Modifying Plate Layouts ............................................................... 210
Removing Plate Layouts from the Database ...................................................... 225
Graphical Data Display and Manipulation...................................................... 226
Detailed Well View .......................................................................................... 226
Applying Data Manipulations to Execute During the Measurement Process........... 228
Applying Data Manipulations to Previously Saved Measurement Data .................. 229
Setting Equations ............................................................................................ 229
Introduction to Quantitative Analysis ................................................................ 270
Creating a Quick Measurement Method Incorporating a Quantitative Analysis ...... 271
Importing QA Objects ...................................................................................... 283
Running a Quick Measurement Method Incorporating Quantitative Analysis ......... 291
Reporting ....................................................................................................... 296
Report Writer.................................................................................................. 296
Standard Reporting-Using Existing Report Templates......................................... 306
Installed Report Templates .............................................................................. 312
Standard Reporting-Using Data Options and Style Options ................................. 333
Data Options and Style Options........................................................................ 343
Advanced Reporting-Using Page Report Objects ................................................ 351
Producing Reports ........................................................................................... 374
Page 3 of 381
Page 4 of 381
EZ Read Microplate Reader Health and Safety
Information
1.1 Safety Instroduction
The EZ Read Microplate Reader Health and Safety Manual cover the following range of microplate
readers:
1. EZ Read 400
2. EZ Read 800
3. EZ Read 800 Plus
4. EZ Read LED
5. EZ Read 2000
The Biochrom EZ Read Microplate Readers are used for microplate-based applications in optically clear
96-well microplates, in addition to -12, -24, -48 and 384-well plates for the EZ Read 2000.
Only trained laboratory personnel should operate the Biochrom EZ Read Microplate Readers. The
Biochrom EZ Read Microplate Readers are intended for general laboratory and research use only.
EZ Read 400 Filters ELISA: 405, 450, 492 & 620nm Research: 405,
450, 492, 562, 595 & 620nm
EZ Read 800 Filters ELISA: 405, 450, 492 & 620nm Research: 405,
450, 492, 562, 595 & 620nm
EZ Read 800 Plus Filters ELISA: 405, 450, 492 & 620nm Research: 405,
450, 492, 562, 595 & 620nm
EZ Read LED Filters ELISA: 405, 450, 492 & 620nm UV: 340, 405,
450, 492, 562 & 595
EZ Read 2000 Monochromator (340-800nm) N/A
Page 5 of 381
EN61326-1:2006 Electromagnetic compatibility*
EN ISO 12100:2010 Safety of machinery –General principles for design, risk assessment and
risk reduction
*These instruments have been tested and found to comply with the limits defined for a CLASS A,
digital device, pursuant to part 15 of the FCC Rules
Safety Symbols:
Warning
High Voltage
Biohazard
High Voltage
High voltages exist inside these instruments. Do not remove covers whilst connected to the
mains supply.
Repair, maintenance and service should only be carried out by individuals trained specifically to
work on these instruments and that have been made aware of the potential hazards.
Trained Users
These instruments are intended to be used by individuals trained in and familiar with the use of
plate readers and washers and their associated hazards. In the event of a malfunction or hazard
occurring, disconnect the unit from power and isolate for decontamination and /or repair.
Lamp Source
Lamp sources used within the reader units produce a light beam that passes through the well
positions and is normally confined within the instrument. The unit should not be operated with
the covers removed as prolonged exposure to the beam intensity and potential UV content of
the beam could cause eye damage.
Page 6 of 381
Personal Protective Equipment
There are no bio-hazardous materials within the instrument; however, this microplate reader
may well be used with bio-hazardous samples. Before using the instrument the user should have
in place decontamination procedures designed to protect laboratory workers from occupationally
acquired infections. A set of suggested decontamination procedures microplate readers are
provided in this manual.
Always read cautions and warnings supplied with assay kits reagents and samples
Decontamination. Equipment should be maintained in a clean state. Equipment returned
for repair should include an appropriate decontamination certificate (refer to website:
http://www.biochrom.co.uk/content/1/65/returns.html)
It is the responsibility of the laboratory manager to ensure that the user of the instrument
is provided with a safe working environment.
Any chemicals used with the microplate reader should be used, stored and disposed of in
accordance with manufacturer’s guidelines and local safety regulations.
Toxic Fumes. Efficient laboratory ventilation must be provided when working with volatile
solvents or toxic substances.
Waste disposal. Disposal of some solvents and chemicals may be classed as hazardous
waste and must be dealt with in accordance with local regulatory practice.
Personal protective equipment including but not limited to gloves, laboratory coats and
safety glasses is recommended when using this instrument. A local risk assessment
should be performed to determine the extent of required PPE.
Changes or modifications
Any changes or modifications made to the instrument could void the user’s authority to operate the
instrument.
If the instrument is operated in a manner not specified, then the protection provided by the
equipment may be impaired and the instrument warranty withdrawn.
Page 7 of 381
1.4 Instrument Validation
An optional check plate (refer to Biochrom website for further information regarding microplate reader
accessories: http://www.biochrom.co.uk/subsubcategory/41/accessories.html) can be used for
instrument validation. Specific check plates are applicable for different EZ Read models (refer to the
appropriate microplate reader user guides). Additional tips include incorporating controls of known
concentrations to validate absorbance measurements.
EZ Read 400 EZ Read 800 EZ Read 800 Plus EZ Read LED EZ Read 2000
Ambient temperature 15°C - +40°C 10°C - +35°C 10°C - +350°C 18°C - +48°C 10°C - +35°C
(operation) (operation) (operation) (operation) (operation)
25°C - +50°C 25°C - +50°C 25°C - +50°C 40°C - +70°C 25°C - +50°C
(storage) (storage) (storage) (storage) (storage)
Fuse 3 A (UK power 3.15A TH 250VAC 3.15A TH 250VAC 3 A (UK power 3.15A TH 250VAC
plug only) plug only)
Outer lighting Precaution, avoid Precaution, avoid Precaution, avoid Precaution, avoid Precaution, avoid
influences direct sunlight direct sunlight direct sunlight direct sunlight direct sunlight
PC connection Standard cable, USB A to USB B USB A to USB B USB A to USB B USB A to USB B
USB A to B cable mini cable mini cable mini cable mini cable
Relative humidity 15 - 85% non 0 to 80 % (Non 0 to 80 % (Non 0 to 90 % (Non 5 to 95%, non
condensing condensing) condensing) condensing) condensing
(operation) (storage only)
Humidity 5 to 95%, Humidity <95%, Humidity 5 to
< 95% non- non-condensing non-condensing 95%, non-
condensing (storage only) (storage only) condensing
(storage) (storage only)
Warming-up time None required None required None required None required None required
Weight 6.6 kg (No special 12 kg (No special 12 kg (No special 7.2 kg (No 10 kg (No special
instructions are instructions are instructions are special instructions are
required for lifting required for lifting required for lifting instructions are required for lifting
or moving the or moving the or moving the required for lifting or moving the
instrument) instrument) instrument) or moving the instrument)
instrument)
Note: There are no user replacebale parts (except for replacement of fuses).
Page 8 of 381
1.6 Technical Specifications
EZ Read 400 EZ Read 800 EZ Read 800 Plus EZ Read LED EZ Read 2000
Lamp Source Tungsten halogen Tungsten halogen Tungsten halogen LED Tungsten halogen
Measurement 0-3.3 OD 0-3.4 OD 0-3.4 OD 0-3.4 OD 0-3.2 OD
range
Reproducibility / 0.25% at 1.0 OD 0.5% 0.1-2.5 OD 0.5% 0.1-2.5 OD 0.5% and 0.005OD 0.8% and 0.005 OD
Precision) at 450 nm to 3.5OD from 0.10-2.0 OD at
450 nm
Accuracy 0.5% at 1.0 OD at 1% from 0.100-2.5 1% from 0.100-2.5 <=1% and 0.005 to 0.5% and 0.005 OD
450 nm OD OD 3.5OD from 0.1-1.0 OD at
450 nm;
1.0% and 0.010 OD
from 1.0-2.0 OD at
450 nm
Standard Filters: 405, 450, 492 and 405, 450, 492 and 405, 450, 492 and 405, 450, 492, None
620nm for ELISA 620nm for ELISA 620nm for ELISA 620nm LED
reader 405, 450, reader 405, 450, reader 405, 450,
492, 562, 570, 595 492, 562, 570, 595 492, 562, 570, 595
and 620 for and 620 for and 620 for
Research reader Research reader Research reader
Wavelngth Range 400-750nm 400-750nm 400-750nm 340- 900nm 340-800nm
Plate Types Flat, round and v- Flat, round and v- Flat, round and v- Flat, round and v- 12, 24, 48 and 96-
bottomed 96-well bottomed 96-well bottomed 96-well bottomed 96-well well plates with
plates plates plates plates standard ANSI/SBS
footprint
Data Output Export to PC Export to PC Export to PC Export to PC Export to PC
Detection System Single channel 8 silicon 8 silicon 8 silicon 2 silicon diodes: one
silicon photodiode photodiodes photodiodes photodiodes for measurement,
one for reference
Reading Speed 25 seconds <5 seconds <5 seconds 5 seconds 35 seconds
Shaking None 4 speed standard 4 speed standard 4 speed standard Linear shaking
Tempertaure None None None None None
Control
Linearity 0.25% and 0.0025 0.25% and 0.0025 0.25% and 0.0025 0.5% and 0.005OD 0.5% and 0.005 OD
OD from 0.1 -2.5 OD from 0.1 -2.5 OD from 0.1 -2.5 to 3.5OD from 0.10-1.0 OD at
OD at 492 nm OD at 492 nm OD at 492 nm 492 nm 1.0% and
0.010 OD from 1.0-
2.0 OD at 492 nm
Computer interface USB 2.0 USB 2.0 USB 2.0 USB 2.0 USB 2.0
Optical system Filters Filters Filters Filters Monochromator
Validation Optional 2010 Optional Asys Optional Asys Optional 2010/2020 Optional Asys
check plate Check plate Check plate plate Check plate
Mode of operation PC control PC control Local or PC control PC control PC control
Analysis software Galapagos Galapagos Galapagos Galapagos Galapagos Software
Software Software Software Software
Page 9 of 381
1.7 Unpacking the EZ Read Microplate Reader
Note: The original packing has been especially designed to protect the instrument during
transportation. It is therefore recommended to keep the original carton with its foam parts and the
accessories box for re-use in case of future shipments. Warranty claims are void if improper packing
results in damage during transport.
1. Check the box for any visible damage during transportation. In case of damage inform your
supplier immediately and keep the damaged packing.
2. Place the device on a suitable working surface.
3. Remove the transportation lock (foam part) from the plate holder. The readers are also supplied
with a metal clip which also requires removal.
2. Connect the instrument to a computer or laptop and connect by clicking the ‘Find Instruments’
icon which detects the respective instrument. For subsequent use users can click the ‘Connect’
icon for recognition
Page 10 of 381
3. Click ‘Quick Measurement’
4. For sample measurements, select the appropriate measurement mode (Single, Dual or Multi-
wavelength). Dual wavelength refers to the measurement of a sample at one wavelength and
that absorbance from another wavelength will be subtracted. Multi-wavelength refers to
absorbance measurements at different wavelengths
Page 11 of 381
7. When users click onto a well, it is highlighted (dashed lines). In regards to dual wavelength
measurements, three absorbance values are displayed
The bold value refers to the absorbance measurement after wavelength subtraction
The second value refers to the absorbance value measured at a desired wavelength
The third value refers to the absorbance value measured at a reference wavelength
8. Results can be saved to ‘Database’. A database is useful for saving, sharing and extracting data
via communication with an external database system (LIMS). Users can save files and
templates onto the database, ‘File’ (save to own personal file), or ‘Save Method Template’
(saves the method protocol for future use)
Page 12 of 381
9. Results can also be exported as Excel, Extended Metafile, results exported as a HTML file, PDF,
Rich Text File, Text File, Word File and XPS File
2.0 Troubleshooting
The website is frequently updated with technical and supplications support information.
Readings are higher or lower Check to see if samples are cloudy or mixed properly. If the sample is not mixed
than expected properly, sediments can settle at the bottom of the well which can lead to
measurement discrepancies.
Check for bubbles in solution.
Check plate orientation.
Check for poor, scratched plates.
Check if the correct plate format is used (96 well plate, flat, round and v-bottomed well
formats with standard ANSI SBS footprint).
Check for condensation on plate base.
If filters have been changed check that the filter positions have been entered and
Page 13 of 381
PROBLEM POSSIBLE CAUSE
calibrated correctly
Check assay preparation steps have been followed correctly.
Check correct sample volume has been dispensed. This is important as pathlength
(which is used to calculate sample concentration using Beer’s Law) is not standardised
and is dependent on sample volume. Therefore the volume must be equal throughout
the plate.
Readings have poor repeatability Check plate types used are suitable.
and are random or noisy
Check that plate transport passes start up checks. This refers to when the instrument
finds the home position of the plate immediately after being switched on. If the plate
reader has a display the status of the check is shown.
Check for any bubbles or wells where there is foam (likely to arise from pipetting or
shaking).
Use a background wavelength correction. For example measure the sample
absorbance at 405nm and wavelength reference at 620nm.
Check sample dilutions are such as to produce a response within the range 0.1 to 2.5
A. This is the recommended linear range of the plate readers.
Check assay preparation steps have been followed correctly.
Check correct sample volume has been dispensed, as mentioned above.
Recommended good laboratory Use a polystyrene plate with no scratches or evaporation which may affect absorbance
practice readings.
Check that pipettes (single and/or multi-channel) dispense the correct set volume.
Check that the correct tips are used for the appropriate pipettes.
Check plate for any bubbles or foam as mentioned previously.
Check readings with a QC plate (refer to user manual for specified plate) – refer to
section 1.4.
Please Note: Before the reader can be returned to base for service, it must be disinfected and a
Declaration of Decontamination Certificate must be completed. This document can be downloaded
from the Biochrom website: http://www.biochrom.co.uk/content/1/65/returns.html
Page 14 of 381
The instrumentation will not be accepted for servicing or return until the above form is completed
fully. Instrumentation that has not been cleaned sufficiently or decontaminated may be subject to
additional charge.
This symbol can be found on the outside of the instrument. It means that the Biochrom EZ Read
Microplate Reader cannot be disposed of in municipal waste. The instrument must be decontaminated
as detailed in part 2.0 of this section
E-mail: support@biochrom.co.uk
Telephone: +44 (0)1223 427890
Fax: +44 (0)1223 427857
Page 15 of 381
Galapagos Expert
Version 1.1.2.0
Page 16 of 381
Software Licence Agreement
1. DEFINITION: This is BIOCHROM LTD’s (BIOCHROM) Software Licence Agreement (the
“Agreement”) which will govern your use of the Biochrom software product(s) contained in this
package (the “Software”).
2. LICENCE: BIOCHROM hereby grants you, and you accept a limited software licence subject to
the terms and conditions contained herein to use the Software. You may only use the Software
on a maximum of one computer at any one time where a computer means a single computer,
or its temporary replacement, or on a subsequent computer. If you wish to use the Software on
more than the designated number of computers at any one time, you must licence additional
copies of the Software from BIOCHROM.
3. TERM: This agreement commences when you begin to use the Software, and continues in
effect until you return the Software to BIOCHROM. At that time, you must also certify in writing
that you have destroyed any archival copies which you may have recorded on any memory
system or magnetic medium. Any such termination shall be without prejudice to the accrued
rights of the parties.
4. BIOCHROM LTD’S RIGHTS: You acknowledge that the rights to the Software and associated
documentation and other related materials are the sole and exclusive property of BIOCHROM.
By accepting this Agreement, you do not become the owner of the Software, but you do have
the right to use the Software in accordance with this Agreement. You agree to use your best
efforts and take all reasonable steps to protect the Software from unauthorised use, illegal
reproduction or illicit distribution.
5. COPYRIGHT: The Software and its associated documentation are copyrighted. You may make
one copy of the Software and the associated documentation for your own purposes
notwithstanding the requirements of the licence. Other than these you agree that no other
copies of the Software or associated documentation will be made.
6. OTHER RESTRICTIONS: You may not rent or lease the Software, but you may transfer the
rights under this Agreement on a permanent basis providing you transfer all copies of the
Software, and all associated documentation, and that the recipient agrees to the terms of this
Agreement.
7. LIMITED WARRANTY: BIOCHROM warrants for a period of one year from the date of receipt
by you, that the Software will perform substantially in accordance with the accompanying
documentation. BIOCHROM does not warrant that the functions contained in the Software will
meet your requirements or that the operation of the Software will be uninterrupted or error-free
or that defects in the Software will be corrected. To the maximum extent permitted by law,
BIOCHROM declaims all other warranties, express or implied, including but not limited to,
implied warranties of merchantability and fitness for a particular purpose with respect to the
Software, and its associated documentation.
8. SUPPORT AND UPGRADES: BIOCHROM will provide telephone support and advise on
questions of design or implementation for a period of 3 months after delivery. In addition but
notwithstanding the limited warranty BIOCHROM will provide any version upgrades issued for
maintenance purposes free of charge during the warranty period. Any further support will be
the subject of a separate maintenance quotation and contract. To obtain support and upgrades
users must register the purchase with BIOCHROM directly.
9. CUSTOMER REMEDIES: BIOCHROM entire liability and your exclusive remedy shall be at
BIOCHROM option, either (a) return of the price paid or (b) repair or replacement of the
Software that does not meet BIOCHROM limited warranty and is returned to BIOCHROM with a
copy of your receipt. This limited warranty is void if failure of the Software has resulted from
damage, accident, abuse or misapplication.
Page 17 of 381
10. LIABILITY: To the maximum extent permitted by applicable law, BIOCHROM and its agents
shall not be liable for any other damages whatsoever (including, but not limited to, damages for
loss of business profits, business interruption, loss of business information, or other pecuniary
loss) arising out of the use or inability to use the BIOCHROM product, even if BIOCHROM or its
agents have been advised of the possibility of such damages. In any case, BIOCHROM entire
liability under any provision of this Agreement shall be limited to the amount actually paid by
you for the Software.
11. TERMINATION OF AGREEMENT: If any of the terms and conditions of this Agreement is
broken, BIOCHROM has the right immediately to terminate in writing the Agreement and
demand that you return the Software to BIOCHROM. At that time, you must also certify in
writing that you have not retained any copies of the Software.
12. GOVERNING LAW: This Agreement is to be governed by, and interpreted in accordance with
the laws of England. Any terms and conditions of this Agreement found to be unenforceable will
be deleted, but will not alter the remaining terms and conditions of this Agreement. The
exclusive jurisdiction of an English court of law shall apply in the event of any dispute
13. ENTIRE AGREEMENT: This Agreement constitutes the entire Agreement between you and
BIOCHROM relating to the licensing of the Software, and applies to you if purchased for your
own use, or to you, your company and the company’s employees if purchased for company use.
No variation or amendment of or addition to the terms and conditions of the Agreement shall be
effective unless prior agreement is obtained in writing from BIOCHROM.
Page 18 of 381
How to get Help
To display tooltips:
o Hover the mouse cursor over the ribbon buttons
Concise explanations of the button are given
While working with Galapagos you may wish to consult the application online help topics or the
application manual for clarification or information on a certain function or option.
Page 19 of 381
2. Click on the Help icon
or
o Click on Help -
or
o Press F1 at any time
Page 20 of 381
To display the manual:
o Display the Help tab and click on Manual
or
o Select Manual from the help drop-down
Page 21 of 381
Display 'About' Information
2. Click About
Keyboard shortcut: Alt, H, A
The 'About' dialog is displayed
Page 22 of 381
or
Selecting About from the Help drop-down
or
1. Click on the File tab and click Help
Page 23 of 381
Contact Biochrom Limited
Biochrom Limited
22 Cambridge Science Park
Cambridge
CB4 0FJ
UK
Tel: +44 (0)1223 423723
www.biochrom.co.uk
Technical Support:
Tel: +44(0)1223 427890
support@biochrom.co.uk
Sales:
Tel: +44 (0)1223 423723
enquiries@biochrom.co.uk
Page 24 of 381
User Interface Overview
The Galapagos user interface is composed of a main application window with a ribbon interface and a
data window where acquired data can be displayed.
The currently logged in user, the current instrument connection status and database connection status
are shown in the status bar at the bottom right of the application:
Instrument connected
Page 25 of 381
Instrument not connected
Instrument details shown when the mouse is hovered over connection status
Database is connected
Database details shown when the mouse is hovered over database status
See also:
o Ribbons
o Data Window
Page 26 of 381
Starting the Application
To start Galapagos:
1. Select Start > All Programs > Biochrom Limited > Galapagos > Galapagos
You can also start the application by double clicking on the Galapagos icon on the Desktop
It is possible to have open multiple instances of the application
Application Ribbons
Galapagos has four ribbons which are always shown and through which all application options can be
accessed. These are:
o File
o Setup
o Methods
o Help
Page 27 of 381
The File tab contains the following:
o Open
o Save As
o Recent
o New
o Print
o Export
o Help
o Copy
o Options
o Exit
Page 28 of 381
The setup tab is shown by selecting Setup or pressing Alt, S
Page 29 of 381
The Help tab is shown by selecting Help or pressing Alt, H
It is possible to have multiple data files open at any time in Galapagos. In addition, it is possible to
open more than one instance of a single file.
Page 30 of 381
With multiple files open you can also select which file to display by clicking the window selection
button and selecting the graph to show:
To Close a File:
1. Click on the tab of the file to be closed
Page 31 of 381
The properties for the current file are displayed:
Note: It is not possible to edit or delete information in the Method Properties view
Page 32 of 381
The groups for the current layout are displayed:
Page 33 of 381
The plotted data is displayed:
Note: Not all well data can be plotted as a chart. In this case, 'Insufficient Data to Chart' is
displayed in the chart view.
To View a Well's Data in Tabular Format for the Current Results File:
1. Select the file whose data you wish to display
2. Select the well of interest
3. Click the Data tab
Page 34 of 381
The data is displayed:
To exit Galapagos:
Page 35 of 381
1. Select the File tab
2. Select Exit
The application is closed.
Page 36 of 381
Data Management
Galapagos can store results data in a database or save to disk files. The following topics are detailed in
this section:
o New
o Open
o Save As
o Database connection and management
o Import
o Export
o Print
o Copy
o Recent
o Options
Page 37 of 381
New
1. Click on New
2. Click on the required method from those available
3. The corresponding acquire tab for the chosen method is displayed
Page 38 of 381
Open
2. Click on Open
3. Click on Open Results from File
4. From the dialog that is displayed, select the required file and click Open
The data is displayed in a new tab in the data window
Page 39 of 381
To open a data source from a database:
1. Select the File tab
2. Click on Open
3. Click on Open Results from Database
or
Launch the Open from Database dialogue from the quick access toolbar by clicking on the
Page 40 of 381
4. Select the result to be opened from the list displayed
Together with the results name, the dialog specifies the method that was used to acquire that
data and the date the data was created
Single and multiple results can be selected by using the Shift and Ctrl keyboard buttons
Each result is displayed in a new tab in the data window
Note: It is not possible to open data from an empty database. If attempted, a warning dialog is
displayed.
See also:
o Applying data manipulations to previously saved data
Page 41 of 381
Save As
2. Click on Save As
3. Click on Save to Database
Page 42 of 381
4. Enter the results name and Click OK
Note: The results name must be unique. If an attempt is made to store a result with the same
name as an existing result an error message is displayed.
Note:In order to save data to a database, Galapagos must be connected to a database. For
help on connecting to a database, refer to the help section on database connection and
management.
Page 43 of 381
Saving data to a file:
1. Select the File tab
2. Click on Save As
3. Click on Save to File
Page 44 of 381
4. Enter the file name and select the file location and click on Save
Page 45 of 381
Database requirements:
Galapagos is designed to work with a database. The database can be located locally or across a
network. If you do not already have a suitable accessible database connection then it is recommended
that you allow the application to create a local Microsoft SQL Server Express 2008 database for you.
The software is designed to work with databases supporting the Structured Query Language (SQL) but
you will only be able connect to an existing database if you are a user on the system and have the
appropriate connection knowledge. Please contact your database manager for support.
Select Automatic Database Connection to connect to SQL Server Express and create a
database called Galapagos for data storage
2. If the database connection is unsuccessful, a connection error dialog is displayed
Page 46 of 381
3. Select whether to attempt manual database configuration or proceed to work offline
Note: The automatic database connection will only connect to servers which have names in
the following format: [Computer Name]\SQLEXPRESS. Additionally, when configured
automatically, Windows Authentication is used. To use a server with a different name or to
use SQL Server Authentication, select Manual Database Configuration.
Note: When working offline, all results are saved to disk file.
Select Manual Database Configuration to manually select the database server and database
name to use
1. Galapagos will search for available database servers
2. If the required server has not been found, type in the name of the server in the Server edit
box
3. Choose which type of authentication to use and click OK
Windows authentication: Windows users can logon to the database
SQL Server authentication: Enter a valid SQL server user name and password combination
Page 47 of 381
4. Enter the name of the database to connect to and click OK
Page 48 of 381
Disconnecting from a database:
Note: When a database is not connected, results data is saved to disk file.
Galapagos will attempt to connect to the last used database on start-up, unless always work offline
has been selected.
To reconnect to the last used database:
1. Select the Setup tab
Page 49 of 381
2. Click on Connect to Database
Page 50 of 381
4. If the required server has not been found, type in the name of the server in the Server edit
box
Page 51 of 381
6. Select the database from the list of available databases and click OK
Page 52 of 381
4. If the required server has not been found, type in the name of the server in the Server edit
box
Page 53 of 381
3. Enter the name of the database to be created and click OK
Note: The standard rules for the format of database names apply. These are summarised
below.
The first character must be one of the following:
o A letter as defined by the Unicode Standard 3.2. The Unicode definition of letters includes
Latin characters from a through z, from A through Z and also letter characters from other
languages
o The underscore (_), at sign (@) or number sign (#)
Subsequent characters can include the following:
o Letters are defined in the Unicode Standard 3.2
o Decimal numbers from either basic Latin or other national scripts
o The at sign (@), dollar sign ($), number sign or underscore (_)
o Embedded spaces, special characters or supplementary characters are not allowed
Page 54 of 381
Upgrading the database:
1. When a Galapagos software upgrade has been installed and a database upgrade is required, the
following message is displayed when Galapagos is started.
Note: It is good practice to backup all data before performing a database upgrade.
Page 55 of 381
Import
Several data formats can be imported into Galapagos, including:
o Text files
o KPL files (Kontrol Plus software file containing measurement data)
2. Click on Import
3. From the list of options available, select the format of the data to be imported by clicking on the
corresponding icon
Page 56 of 381
4. Select the file to import and click Open
Note: If the data file imported comprises multiple data sets, each data set will be opened into a
separate data window.
Export
Measurement, instrument and manipulated data can be exported to several data formats, including:
o Microsoft Excel
o Extended metafile
o HTML
o PDF
o Rich text format (RTF)
o Text
o Microsoft Word
o XPS
Page 57 of 381
The following information is exported. Only sections appropriate to the data are included:
o Method
o Method type
o Originator
o Date created
o Settings
o Wavelengths
o Measurement mode
o Shaking mode settings
o Timing settings
o Equations
o Data manipulation algorithms applied to the measurement data
o Qualitative Analysis
o Details of the QA object
o Standard details and statistics
o Coefficient and goodness of fit parameters
o Results
o Date & time
o Result Validity
o Data Validity
o Operator
o Instrument type
o Instrument serial number
o Firmware version
o Layout
o Plate Definition
o Plate Layout
o Group assignments
o Data
o Measurement data and results of data manipulations
For the export functions to be enabled, there must be measurement data open in the software.
Page 58 of 381
To Exporting Data to a File:
1. Select the File tab
2. Click on Export
3. From the list of options available, select the format of the data to be exported by clicking on the
corresponding icon
Page 59 of 381
4. Enter the file name and location and click Save
Note: When exporting to Excel, the measurement data and manipulated data is written to a
separate worksheet.
See Also
o File tab Options for export options
Page 60 of 381
Export Options
Options are available to set the page format (orientation) and the list separator type when exporting
data.
2. Click on Options
Page 61 of 381
3. Select one of the options from the Page Format drop down list
Note: This option does not apply to the export to Microsoft Excel or text file formats
Page 62 of 381
To change the list separator:
1. Select the File tab
2. Click on Options
Page 63 of 381
3. Select one of the options from the List Separator drop down list
Note: The List Separator option only applies to the text file formats and Copy command
Page 64 of 381
Print and Print Preview
Page 65 of 381
To print the current method results and settings:
1. Open or show the file containing the results and settings to print
2. Select the File tab and click on Print
3. Click Print
See Also
o File tab Options for page format options
Page 66 of 381
Copy
3. Click on Copy
Page 67 of 381
Recent
Recently opened results data can be quickly accessed through the Recent option. This applies to
results data stored in a database or saved to disk files if working offline.
Page 68 of 381
Data Validity
When Galapagos measurement data is opened, Galapagos uses a data integrity routine to check that
the results file has not been altered since it was last viewed in Galapagos. The outcome of this data
validity routine is displayed in the Results section of the Method Properties pane.
Page 69 of 381
Instrument Management
Galapagos can be used to connect to a variety of different instruments. For more information relating
to the configuration of Galapagos for use with your instrument please see the following topics:
o EZ Read Models
o Anthos Models
o ASYS Models
Connecting to an Instrument
Page 70 of 381
3. Select the instrument to connect to from the instruments available
Note: Where only one instrument is found, Galapagos will automatically connect to it.
Galapagos cannot automatically identify some types of instrument. When selected, such
instruments require the user to identify the instrument type from the options available.
Galapagos will store this information for future use.
Page 71 of 381
Connecting to the last used instrument:
When launched, Galapagos will automatically connect to the last used instrument if available. If the
instrument is not available, the connection error dialog is displayed.
2. Click on Connect
Page 72 of 381
To disconnect from an instrument:
1. Select the Setup tab
2. Click on Disconnect
Page 73 of 381
4. Select the instrument to connect to from the instruments available
Note: Where only one instrument is found, Galapagos will automatically connect to it.
Galapagos cannot automatically identify some types of instrument. When selected, such
instruments require the user to identify the instrument type from the options available.
Galapagos will store this information for future use.
Page 74 of 381
EZ Read Models
The topics available in this section are:
Instrument Connection
Instrument Window
Instrument Properties: General tab (status, filters, acquire raw energy, data and load & eject
plates)
Instrument Properties: Methods and Plate Data tab
Instrument Properties: Plate Definitions tab
Instrument properties: Transport
Instrument Properties: Wavelength Calibration tab
Note: The instrument type connected will determine which instrument property tabs are
accessible.
Page 75 of 381
Instrument Window
Page 76 of 381
2. Click the Instrument group dialog box launcher -
Keyboard shortcut: To show the Instrument properties, press ALT, S, I
See also:
o Instrument Properties: General
Page 77 of 381
Instrument Properties: General
The General tab of the Instrument Property page displays details about the connected instrument and
allows certain instrument functions to be executed.
The following topics are covered in this section:
Displaying the general tab
Modifying the instrument's filter settings
Performing an absorbance linearity calibration of all the instrument's filter set
Acquiring raw energy data
Loading and ejecting a plate
Page 78 of 381
To show the instrument general properties page:
1. Open the instrument property sheet
2. Click the General tab
The status information displayed is for information only and cannot be modified
Page 79 of 381
2. Enter the corresponding filter wavelength
Note: All available filter positions are shown. It is not necessary to have filters installed in all
available filter positions. The occupied filter positions do not need to be contiguous.
3. Click Apply
If any filter details have been modified, the filter absorbance linearity calibration routine is
performed for those filter positions. This can take several minutes to complete.
Note: The instrument general property page shows at which filter positions the instrument has
filters installed and their corresponding wavelengths. The instrument cannot detect any filter
position changes made by the user so if any filter positions are changed or added then the filter
list must be updated.
Page 80 of 381
2. Click on Acquire Raw Energy
The raw energy measurement dialogue is displayed whilst the data is acquired.
Page 81 of 381
To load a plate:
1. Click on Load Plate
To eject a plate:
1. Click on Eject Plate
The Methods and Plate Data tabs of the Instrument Property page allows instrument stored methods
and plate results to be downloaded to Galapagos and instrument compatible methods to be uploaded
to the instrument from Galapagos. Note that these features are only available when connected to
instrument types that support the transfer of methods and plate data.
The following topics are covered in this section:
Downloading methods from the instrument to Galapagos
Uploading methods to the instrument
Downloading results data from the instrument to Galapagos
All topics require connection to an instrument that supports the transfer of method and plate data to
Galapagos, such as the EZ Read 800 Plus.
Page 82 of 381
3. Click on the Methods tab
Page 83 of 381
4. Click on Download and enter a file name to save the data
Note: The method files are saved in the KMT file format.
Page 84 of 381
5. The methods that have been downloaded are displayed in the methods tab
Page 85 of 381
3. Click on the Methods tab
Page 86 of 381
2. Click on Upload and select the methods file to upload
The Upload Methods dialogue is displayed during the file upload process:
Page 87 of 381
To download results data from the instrument:
1. Select the Setup tab
Page 88 of 381
4. Click on Download
The downloaded data sets are displayed and saved as text files:
The Plate Definitions tab of the Instrument Property page allows instrument stored plate definitions to
be downloaded to Galapagos, modified and uploaded to the instrument. Note that these features are
only available when connected to instrument types that support the transfer of plate definition
information.
The following topics are covered in this section:
Downloading plate definition data from the instrument
Editing plate definitions and uploading to the instrument
All topics require connection to an instrument that supports the transfer of plate definition of data to
Galapagos, such as the EZ Read 2000.
Page 89 of 381
To download plate definition data from the instrument:
1. Select the Setup tab
The size, column & row offsets and columns & row spacing are displayed for each plate
definition.
Page 90 of 381
To edit a plate definition and upload to the instrument:
1. Download the plate definitions from the instrument
2. Click on the variable to edit and enter the value required.
3. Click on Upload
The edited plate definition data is uploaded to the instrument
The Transport tab of the Instrument Property page reports status information for the X and Y plate
transport drives and the wavelength drive. Note that these features are only available when connected
to instrument types that support the reading of this information.
A connection is required to an instrument that allows Galapagosto read drive information from the
instrument, such as the EZ Read 2000.
Page 91 of 381
3. Click on the Transport tab
The Wavelength Calibration tab of the Instrument Property page enables a wavelength calibration of
the instrument to be performed. Note that these features are only available when connected to
instrument types that support wavelength calibration.
The following topics are covered in this section:
Wavelength recalibration using the inbuilt reference LED only
Wavelength recalibration using the inbuilt reference LED and Holmium filter
Moving to a specific wavelength
All topics require connection to an instrument that supports wavelength recalibration, such as the EZ
Read 2000.
Page 92 of 381
To perform a wavelength recalibration using the inbuilt reference LED only:
1. Select the Setup tab
4. Click on Recalibrate
The instrument performs the calibration routine and recalibrates the wavelength. The
instrument's status information is updated.
5. Click OK
Page 93 of 381
To perform a Wavelength recalibration using the inbuilt reference LED and Holmium filter:
1. Select the Setup tab
4. Click on the Use Holmium Filter check box and click on Recalibrate
The instrument performs the calibration routine and recalibrates the wavelength. The
instrument's status information is updated.
5. Click OK
Page 94 of 381
To move to a specific wavelength:
1. Select the Setup tab
4. Enter the required wavelength in the Wavelength edit field and click on Go To Wavelength
The instrument is set to the required wavelength. The instrument's status information is
updated.
5. Click OK
Page 95 of 381
Anthos Models
The topics available in this section are:
Instrument Connection
Instrument Window
Instrument Properties: General (status and filters)
Instrument Window
To display the Instrument Window:
1. Click on the Instrument tab below the data window
Page 96 of 381
2. Click the Instrument group dialog box launcher -
Keyboard shortcut: To show the Instrument properties, press ALT, S, I
See also:
o Instrument properties: General
Page 97 of 381
Instrument Properties: General
The General tab of the Instrument Property page displays details about the connected instrument and
allows certain instrument functions to be executed.
The following topics are covered in this section:
Displaying the general tab
Modifying the instrument's filter settings
Performing an absorbance linearity calibration of all the instrument's filter set
The status information displayed is for information only and cannot be modified
Page 98 of 381
To modify the instrument's filter settings:
The instrument general property page shows at which filter positions the instrument has filters
installed and their corresponding wavelengths. The listing can be updated to reflect a change in the
instrument's filter setup
1. Click in the filter position's check box to indicate a filter is installed in that filter position
2. Enter the corresponding filter wavelength
Note: All available filter positions are shown. It is not necessary to have filters installed in all
available filter positions. The occupied filter positions do not need to be contiguous.
3. Click Apply
If any filter details have been modified, the filter absorbance linearity calibration routine is
performed for those filter positions. This can take several minutes to complete.
Note: The instrument general property page shows at which filter positions the instrument has
filters installed and their corresponding wavelengths. The instrument cannot detect any filter
position changes made by the user so if any filter positions are changed or added then the filter
list must be updated.
Page 99 of 381
ASYS Models
The topics available in this section are:
Instrument Connection
Instrument Window
Instrument Properties: General tab (status, filters, acquire raw energy, data and load & eject
plates)
Instrument Properties: Methods and Plate Data tab
Instrument Properties: Plate Definitions tab
Instrument properties: Transport
Instrument Properties: Wavelength Calibration tab
Note: The instrument type connected will determine which instrument property tabs are
accessible.
Instrument Window
To display the Instrument Window:
1. Click on the Instrument tab below the data window
See also:
o Instrument properties: General
o Instrument properties: Method and Plate Data
The General tab of the Instrument Property page displays details about the connected instrument and
allows certain instrument functions to be executed.
The following topics are covered in this section:
Displaying the general tab
Modifying the instrument's filter settings
Performing an absorbance linearity calibration of all the instrument's filter set
Acquiring raw energy data
Loading and ejecting a plate
The status information displayed is for information only and cannot be modified
Note: All available filter positions are shown. It is not necessary to have filters installed in all
available filter positions. The occupied filter positions do not need to be contiguous.
3. Click Apply
If any filter details have been modified, the filter absorbance linearity calibration routine is
performed for those filter positions. This can take several minutes to complete.
Note: The instrument general property page shows at which filter positions the instrument has
filters installed and their corresponding wavelengths. The instrument cannot detect any filter
position changes made by the user so if any filter positions are changed or added then the filter
list must be updated.
The raw energy measurement dialogue is displayed whilst the data is acquired.
To load a plate:
1. Click on Load Plate
To eject a plate:
1. Click on Eject Plate
The Methods and Plate Data tabs of the Instrument Property page allows instrument stored methods
and plate results to be downloaded to Galapagos and instrument compatible methods to be uploaded
to the instrument from Galapagos. Note that these features are only available when connected to
instrument types that support the transfer of methods and plate data.
The following topics are covered in this section:
Downloading methods from the instrument to Galapagos
Uploading methods to the instrument
Downloading results data from the instrument to Galapagos
All topics require connection to an instrument that supports the transfer of method and plate data to
Galapagos, such as the ASYS Expert Plus.
Note: The method files are saved in the KMT file format.
The Upload Methods dialogue is displayed during the file upload process:
The Plate Definitions tab of the Instrument Property page allows instrument stored plate definitions to
be downloaded to Galapagos, modified and uploaded to the instrument. Note that these features are
only available when connected to instrument types that support the transfer of plate definition
information.
The following topics are covered in this section:
Downloading plate definition data from the instrument
Editing plate definitions and uploading to the instrument
All topics require connection to an instrument that supports the transfer of plate definition of data to
Galapagos, such as the UVM340.
The size, column & row offsets and columns & row spacing are displayed for each plate
definition.
3. Click on Upload
The edited plate definition data is uploaded to the instrument
The Transport tab of the Instrument Property page reports status information for the X and Y plate
transport drives and the wavelength drive. Note that these features are only available when connected
to instrument types that support the reading of this information.
A connection is required to an instrument that allows Galapagosto read drive information from the
instrument, such as the UVM340.
The Wavelength Calibration tab of the Instrument Property page enables a wavelength calibration of
the instrument to be performed. Note that these features are only available when connected to
instrument types that support wavelength calibration.
The following topics are covered in this section:
Wavelength recalibration using the inbuilt reference LED only
Wavelength recalibration using the inbuilt reference LED and Holmium filter
Moving to a specific wavelength
All topics require connection to an instrument that supports wavelength recalibration, such as the
UVM340.
4. Click on Recalibrate
The instrument performs the calibration routine and recalibrates the wavelength. The
instrument's status information is updated.
5. Click OK
4. Click on the Use Holmium Filter check box and click on Recalibrate
The instrument performs the calibration routine and recalibrates the wavelength. The
instrument's status information is updated.
5. Click OK
4. Enter the required wavelength in the Wavelength edit field and click on Go To Wavelength
The instrument is set to the required wavelength. The instrument's status information is
updated.
5. Click OK
Quick Method:
The Quick Measurement application enables you to perform a quick sample check at a specified
wavelegth.
1. Launch from the quick access toolbar by clicking on the Quick Measurement icon -
Note: Certain instrument types eject the plate when a method type is selected.
See also:
o Acquiring using Quick Measurement
Note: The wavelengths available for selection vary according to the instrument type connected.
Some instrument types have a limited set of discrete wavelengths available for selection and
other instrument types have available for selection a continuous range of wavelengths.
Note: If the wavelength entered is not a permitted value, it is automatically changed to the
nearest permitted value when the measurement is started.
5. Select the Manipulate tab from the Method Tools context group
6. Click on Change Plate Layout
To return to the Acquire tab without selecting a plate layout, click on Discard Layout
Note: The acquisition of data cannot be started if the Layout tab remains open. Return to the
Acquire tab by clicking Accept Layout or Discard Layout.
Note: On accepting a plate layout, any data previously acquired and displayed will be cleared
from the display.
8. Select the Acquire tab from the Method Tools context group and click Start
Note: For measurements involving more than one physical plate, prompts will request the
correct plate is loaded before the measurement is started
If Stop is clicked during data acquisition, the measurement processes will complete but no
measurement data will either be saved or displayed
10. Once acquisition is complete, the measurements for each well are displayed in the data window
Note: It is not possible to edit any of the measurement values in the data window.
Note: If a well cannot be measured because too much or too little light is passing through it, no
well value is shown.
Note: Data from only the current quick measurement can be displayed. To display multiple
quick measurement data sets, first save the data and then open the required data sets.
12. The acquired data is automatically stored to either the connected database or, if working offline,
to file using the default naming scheme. Additional copies of the data can be saved using the
Save As command in the File tab
Note: It is not possible to change any measurement settings while data acquisition is in
progress.
Note: Certain instrument types eject the plate once the measurement sequence is complete.
Note: The measurement and reference wavelengths must be different. If they are set to be the
same, a warning dialog is displayed.
Note: The wavelengths available for selection vary according to the instrument type connected.
Some instrument types have a limited set of discrete wavelengths available for selection and
other instrument types have available for selection a continuous range of wavelengths.
Note: If the wavelength entered is not a permitted value, it is automatically changed to the
nearest permitted value when the measurement is started.
5. Select the Manipulate tab from the Method Tools context group
6. Click on Change Plate Layout
To return to the Acquire tab without selecting a plate layout, click on Discard Layout
Note: The acquisition of data cannot be started if the Layout tab remains open. Return to the
Acquire tab by clicking Accept Layout or Discard Layout
Note: On accepting a plate layout, any data previously acquired and displayed will be cleared
from the display.
8. Click Start
If Stop is clicked during data acquisition, the measurement processes will complete but no
measurement data will either be saved or displayed.
10. Once acquisition is complete, the measurements for each well are displayed in the data window
The Equations section of the Method Properties dialogue displays the equation used to calculate
the difference between the measured and reference value. This equation cannot be edited or
removed. For information on managing equations, see the section on graphical data display and
manipulation.
Note: It is not possible to edit any of the measurement values in the data window.
Note: If a well cannot be measured because too much or too little light is passing through it, no
well value is shown.
Note: Data from only the current quick measurement can be displayed. To display multiple
quick measurement data sets, first save the data and then open the data.
11. Select a well to display the well's measurement data in tabular form in the data window
12. The acquired data is automatically stored to either the connected database or, if working offline,
to file using the default naming scheme. Additional copies of the data can be saved using the
Save As command in the File tab
Note: It is not possible to change any measurement settings while data acquisition is in
progress.
Note: Certain instrument types eject the plate once the measurement sequence is complete
entering the required value into the edit field or using the arrows to increment the existing
value. Select the wavelengths to be measured by either selecting the required wavelengths
from the those available or by typing in the required values into the corresponding wavelength
edit fields.
Note: Each measurement wavelength must be different. If two or more are set to be the same
a warning dialog is displayed when Start is clicked.
Note: The wavelengths available for selection vary according to the instrument type connected.
Some instrument types have available for selection a limited set of discrete wavelengths and
other instrument types have available for selection a continuous range of wavelengths.
Note: The minimum number of wavelengths selectable is two. The maximum number of
wavelengths that can be selected depends on the instrument type connected. For instrument
types supporting a limited number of discrete wavelengths, the maximum number of
wavelengths selected cannot be greater than the number of discrete wavelengths supported by
the instrument. For instrument types supporting a continuous range of wavelengths, the
maximum number of wavelengths selected cannot be greater than 10.
Note: If the wavelength entered is not a permitted value, it is automatically changed to the
nearest permitted value when the measurement is started.
Note: The measurements are acquired in the order in which the wavelengths are specified.
5. Select the Manipulate tab from the Method Tools context group
6. Click on Change Plate Layout
To return to the Acquire tab without selecting a plate layout, click on Discard Layout
Note: The acquisition of data cannot be started if the Layout tab remains open. Return to the
Acquire tab by clicking Accept Layout or Discard Layout
Note: On accepting a plate layout, any data previously acquired and displayed will be cleared
from the display.
8. Click Start
Note: For measurements involving more than one physical plate, prompts will request the
correct plate is loaded before the measurement is started
If Stop is clicked during data acquisition, the measurement processes will complete but no
measurement data will either be saved or displayed.
10. Once acquisition is complete, the measurements for each well are displayed in the data window
Note: The absorbance values are plotted from lowest to highest wavelength, irrespective of the
order the wavelengths are specified in Step 4.
Note: It is not possible to edit any of the measurement values in the data window.
Note: If a well cannot be measured because too much or too little light is passing through it, no
well value is shown.
Note: Data from only the current quick measurement can be displayed. To display multiple
quick measurement data sets, first save the data and then open the data.
12. The acquired data is automatically stored to either the connected database or, if working offline,
to file using the default naming scheme. Additional copies of the data can be saved using the
Save As command in the File tab
Note: It is not possible to change any measurement settings while data acquisition is in
progress.
Note: Certain instrument types eject the plate once the measurement sequence is complete
Either follow all the steps below or Open a Method Template and continue from Step 11 below.
Note: The low and high wavelengths must be different. If they are set to be the same, a
warning dialog is displayed.
Note: The step size cannot be larger than the spectral range. A warning dialog is displayed is
the spectral range is less than the step size.
Note: The combination of spectral range and step size selected must allow for there to be at
least two data points in the spectrum. If the settings do not allow this, a warning dialog is
displayed.
Note: If the wavelength entered is not a permitted value, it is automatically changed to the
nearest permitted value when the measurement is started.
5. Select the Manipulate tab from the Method Tools context group
6. Click on Change Plate Layout
To return to the Acquire tab without selecting a plate layout, click on Discard Layout
Note: The acquisition of data cannot be started if the Layout tab remains open. Return to the
Acquire tab by clicking Accept Layout or Discard Layout
Note: On accepting a plate layout, any data previously acquired and displayed will be cleared
from the display.
Note: For measurements involving more than one physical plate, prompts will request the
correct plate is loaded before the measurement is started
10. Once acquisition is complete, the measurements for all wells are displayed in the data window
Note: The spectrum displayed in each well are each thumbnails of the full spectrum obtained
during data acquisition. When a well is selected, the spectrum displayed in the chart window
shows the entire data set.
12. The acquired data is automatically stored to either the connected database or, if working offline,
to file using the default naming scheme. Additional copies of the data can be saved using the
Save As command in the File tab
Note: It is not possible to change any measurement settings while data acquisition is in
progress.
Note: Certain instrument types eject the plate once the measurement sequence is complete
Note: Sample shaking can be incorporated into a quick measurement if the instrument
connected supports shaking.
Either follow all the steps below or Open a Method Template and continue from Step 11 below.
1. Display the Quick Measurement window
2. Select the Manipulate tab from the Method Tools context group
3. Click on Change Plate Layout
To return to the Acquire tab without selecting a plate layout, click on Discard Layout
Note: The acquisition of data cannot be started if the Layout tab remains open. Return to the
Acquire tab by clicking Accept Layout or Discard Layout
Note: On accepting a plate layout, any data previously acquired and displayed will be cleared
from the display.
5. Select the Acquire tab from the Method Tools context group
Note: Not all instrument types that support shaking require the shaking speed to be specified.
Change the duration by selecting the units from the drop down list and either entering the
required value in the edit field or using the arrows to increment the existing value. The
updated duration is displayed. Click anywhere outside the Shaking Duration dialog to set the
duration.
Note: For measurements involving more than one physical plate, prompts will request the
correct plate is loaded before the measurement is started
If Stop is clicked during data acquisition, the measurement processes will complete but no
measurement data will either be saved or displayed.
Note: It is not possible to edit any of the measurement values in the data window.
Note: If a well cannot be measured because too much or too little light is passing through it, no
well value is shown.
Note: Data from only the current quick measurement can be displayed. To display multiple
quick measurement data sets, first save the data and then open the data.
15. The acquired data is automatically stored to either the connected database or, if working offline,
to file using the default naming scheme. Additional copies of the data can be saved using the
Save As command in the File tab
Note: It is not possible to change any measurement settings while data acquisition is in
progress.
Note: Certain instrument types eject the plate once the measurement sequence is complete.
Either follow all the steps below or Open a Method Template and continue from Step 8 below.
1. Display the Quick Measurement window
2. Select the Manipulate tab from the Method Tools context group
3. Click on Change Plate Layout
To return to the Acquire tab without selecting a plate layout, click on Discard Layout
Note: The acquisition of data cannot be started if the Layout tab remains open. Return to the
Acquire tab by clicking Accept Layout or Discard Layout
Note: On accepting a plate layout, any data previously acquired and displayed will be cleared
from the display.
5. Select the Acquire tab from the Method Tools context group
6. Select the measurement mode, the wavelength(s) and shaking conditions (if supported by the
instrument connected and if required)
Enter the required setpoint temperature into the edit field or use the arrows to increment
the existing value.
Note: Instruments that support temperature control have factory set temperature ranges at
which they can operate. This determines the value the setpoint can be set to.
8. Click Start
Note: For measurements involving more than one physical plate, prompts will request the
correct plate is loaded before the measurement is started
If Stop is clicked during data acquisition, the measurement processes will complete but no
measurement data will either be saved or displayed.
Note: It is not possible to edit any of the measurement values in the data window.
Note: If a well cannot be measured because too much or too little light is passing through it, no
well value is shown.
Note: Data from only the current quick measurement can be displayed. To display multiple
quick measurement data sets, first save the data and then open the data.
11. The acquired data is automatically stored to either the connected database or, if working offline,
to file using the default naming scheme. Additional copies of the data can be saved using the
Save As command in the File tab
Note: It is not possible to change any measurement settings while data acquisition is in
progress.
Note: Certain instrument types eject the plate once the measurement sequence is complete.
Either follow all the steps below or Open a Method Template and continue from Step 11 below.
1. Display the Quick Measurement window
2. Select the Manipulate tab from the Method Tools context group
3. Click on Change Plate Layout
To return to the Acquire tab without selecting a plate layout, click on Discard Layout
Note: The acquisition of data cannot be started if the Layout tab remains open. Return to the
Acquire tab by clicking Accept Layout or Discard Layout
Note: On accepting a plate layout, any data previously acquired and displayed will be cleared
from the display.
5. Select the Acquire tab from the Method Tools context group
6. Select the measurement mode, the wavelength(s) and shaking conditions (if supported by the
instrument connected and if required)
8. Set the length of the Delay before acquisition begins by clicking on the Delay time arrow
Use of a time delay can be disabled by unchecking the Use Delay option.
The delay time can be entered into the first edit box in the format hours : minutes : seconds or
by using the arrows to increment the existing value in seconds. Alternatively, the delay time
can be entered into the second edit box in the format hours : minutes : seconds or by using the
arrows to increment the existing value in the units selected from the drop down list.
Note: The delay is the time before the first measurement cycle is started. If shaking is enabled,
the delay time is in addition and before an initial shaking time.
Use of an interval time can be disabled by unchecking the Use Interval option.
The interval time can be entered into the first edit box in the format hours : minutes : seconds
or by using the arrows to increment the existing value in seconds. Alternatively, the interval
time can be entered into the second edit box in the format hours : minutes : seconds or by
using the arrows to increment the existing value in the units selected from the drop down
list.
Note: The interval is the time between the start of successive cycles. The minimum value is set
by the cycle time.
Note: The cycle time is determined by the time taken by the instrument to acquire the data for
each cycle and, if selected, the shaking duration if the shaking mode is set to Cycle.
10. Set the duration by clicking on the duration time arrow
The duration is a multiple of the cycle time and is determined by the number of cycles which is
entered in the Total Cycles text field or using the arrows to increment the existing value.
Alternatively, the duration time can be entered into the second edit box in the format hours :
minutes : seconds or by using the arrows to increment the existing value in multiples of the
cycle time. Any value entered that is not a multiple of the cycle time is rounded off to the
nearest multiple of the cycle time.
minutes : seconds or by using the arrows to increment the existing value in multiples of the
cycle time in the units selected from the drop down list. Any value entered that is not a multiple
of the cycle time is rounded off to the nearest multiple of the cycle time.
Note: The cycle time is determined by the time taken by the instrument to acquire the data for
each cycle and, if selected, the shaking duration if the shaking mode is set to Cycle.
Note: For measurements involving more than one physical plate, prompts will request the
correct plate is loaded before the measurement is started
If Stop is clicked during data acquisition, the measurement processes will complete but no
measurement data will either be saved or displayed.
For each wavelength measured, the absorbance is plotted against time. The axes of all plots
cover the same range to allow comparison of data between wells.
Note: It is not possible to edit any of the measurement values in the data window.
Note: If a well cannot be measured because too much or too little light is passing through it, no
well value is shown.
Note: Data from only the current quick measurement can be displayed. To display multiple
quick measurement data sets, first save the data and then open the data.
15. The acquired data is automatically stored to either the connected database or, if working offline,
to file using the default naming scheme. Additional copies of the data can be saved using the
Save As command in the File tab
Note: It is not possible to change any measurement settings while data acquisition is in
progress.
Note: Certain instrument types eject the plate once the measurement sequence is complete.
See also:
o Detailed well view
o Applying data manipulations during the measurement process
Note:The layout name and file name must be the same. If the plate layout is saved and the file
name is not the same as the plate layout name, Galapagoswill automatically adjust the name to
be the same as the file name.
Note: The layout name must be unique. If an attempt is made to save the layout with the same
name as an existing layout an error message is displayed.
Note: When saving a plate layout to the database, the corresponding plate definition must have
previously been saved to the database or an identical plate definition must exist in the
database. If this is not the case, a prompt will allow the following options:
Note: Plate layout files are saved with the file extension .layout
Note: The layout name must be unique. If an attempt is made to save the layout with the
same file name as an existing layout an error message is displayed.
3. Select the layout to be opened from the list displayed and click Open
The plate layout is displayed in the active tab in the plate layout display
Note: It is not possible to open data from an empty database. If attempted, a warning dialog is
displayed.
2. Select the layout to be opened from the list displayed and click Open
The plate layout is displayed in the active tab in the plate layout display
3. Click on Yes
Note: If a plate layout is not stored in the database, a warning dialogue is displayed:
3. Select the plate definition file from the database or file list
All plates in the plate layout will be of the type defined by the plate definition file.
4. The Properties tab will show the plate definition details in the Plate Definition entry in the
Layout section.
The entry can be expanded to show all plate parameters using the symbol and reduced to
hide the parameters using the symbol. The fields are read only and cannot be edited.
Note: Instruments are compatible with a limited number of plate definitions. If an incompatible
plate definition is selected a warning message is displayed and the selection rejected.
The group tab updates to show an entry for each plate with the groups assigned to each plate
detailed.
The watermark displayed on the plate indicate its plate number in the plate series
Note: If additional plates are added to the default layout, then the new plates will be created
comprising the same layout. If additional plates are added to a non-default layout, then the
new plates will be created with all wells assigned to a new group of samples wells.
Note: When reducing the number of plates in a layout, the most recently added plate is
removed.
Note: Groups that only appear on a plate which has been removed are deleted from the layout
all together.
The watermark displayed on the plate indicate its plate number in the plate series
Select the group of interest by clicking on the corresponding group name from those listed in
the Group tab
Selecting Wells:
1. To select a single well, click on the well of interest
The keyboard Control key enables well selection methods to be combined. With a well or
set of wells selected, press and hold the keyboard Control key before selecting the next
set of wells. Any combination of the above selection methods is permitted.
Note: Multiple well selection is confined to wells from the same plate. To configure a group to
comprise wells from more than one plate, see Adding Wells to Existing Groups.
Note: Wells on plates that have been assigned as masked wells during the plate's definition
cannot be selected. These masked wells are labelled N/A.
3. Click on Yes
Note: If default group naming is used, when a group is removed from the layout, the groups
using default naming are renumbered so the first of the remaining groups to be added to the
layout is called 'Group '1, the next 'Group 2' and so on.
2. Click on Yes
Note: The Clear Groups command removes all groups from all plates of the layout.
Name: By default, groups are named 'Group n' where n is a number and for the first group
created is 1 and which is incremented by 1 for each subsequent group created. Group names
can be edited by clicking in the name edit field but have to be unique
Description: By default, no description is provided. Click in the description edit field to enter a
description
Well Type: Each group must be assigned one of the four well types from the drop down list. By
default this is set to the Sample option
The border used to highlight the group is coloured according to the well type selected. The
colours are:
Sample: red
Reference: green
Control: blue
Standard: orange
To update the group's well assignment, click on button. This will update the plate layout
display to reflect the revised assignment.
Note: Name, description and well type can be modified using the plate layout property pane.
Note: A well can be part of only one group.
Note: Set group replicates through the Plate Properties pane.
Note: For a group comprising standards, set the concentration of the standards by clicking on
Edit Constant.
Note: Name, description and well type can be modified using the plate layout property pane
Note: A well can be part of only one group
Note: This operation can be performed on plate layouts which comprise multiple plates.
Note: A constant can only be added a an individual well if the well is part of a group.
3. Select whether to add to the group or well using the selection list displayed
4. Enter the name of the constant and, optionally a description, in the Name and Description edit
fields of the Add Constant dialogue
5. Select the type of constant to assign by selecting either Static or Prompted from the Type
drop down list
Note: A static constant always has the same value. The value of a prompted constant is
requested before it is used in a data manipulation.
If a Static constant has been selected, enter the value to be used in the Value edit field
Click OK
2. Select the constant to edit from the list displayed and click OK
Note: The Name, description and value of standard concentrations are added through the Edit
Constants option and standard concentration constants do not appear in Delete Constants list.
Standard concentration constants are automatically added and removed according to the
replicate statistics for each of the groups comprising standards. For additional information, see
Creating a Quick Measurement incorporating Quantitative Analysis.
2. Select the constant to delete from the list displayed and click OK
Note: To remove wells from a group that comprises wells from more than one plate, remove
the necessary wells from each plate separately.
Note: By default, the number of replicates for a group is set to a value of one. The range of
valid values is one to ten.
Note: The replicates run in sequence through the wells.
Note: By default, the number of replicates for a group is set to a value of one. The range of
valid values is one to ten.
Note: The replicates run in sequence through the wells.
Click on OK
Click on Save
See also:
o Opening method template files
Note: All active quick measurement tabs must be closed before attempting to open a method
template
Click on OK
The method is displayed
Note: All active quick measurement tabs must be closed before attempting to open a method
template
Click on OK
The method is displayed
See also:
o Saving method template files
Galapagos provides tools to define plate characteristics and save them for use when taking
measurements.
Each plate definition tab can display a single plate definition, whether newly created or opened
from a previously saved layout. Additional plate definition tabs can be created by repeating
Steps 1 & 2 above.
The Create group enables a new plate definition to be created from the default standard plate
definition. The Database and File groups enable plate definitions to be saved, previously saved
layouts opened and unused plate definitions to be removed from the database.
See also:
o Saving and opening plate definitions
o Creating plate definitions
o Removing plate definitions from the database
Note:The plate definition name and file name must be the same. If the plate definition is saved
and the file name is not the same as the plate definition name, Galapagoswill automatically
adjust the name to be the same as the file name.
Note: The layout name must be unique. If an attempt is made to save the plate definition with
the same name as an existing plate definition an error message is displayed.
3. Enter the file name and select the file location and click on Save
The plate definition is displayed in the active tab in the plate definition display
Note: With the Open from Database dialogue displayed, access the content filter for each field
by moving the mouse over the field name and clicking on the that appears. In the filter
dialogue box that is displayed, select whether to limit the displayed output for the field to those
item(s) selected or not to filter by checking Select All.
Note: It is not possible to open data from an empty database. If attempted, a warning dialog is
displayed.
3. Select the plate definition to be opened from the list displayed and click Open
The plate definition is displayed in the active tab in the plate definition display
If the existing plate definition has not been saved, a prompt will be displayed warning of
possible data loss. Click Yes to continue.
Note:For details of how to save a plate definitions, see Saving and Opening Plate Definitions.
purposes. Click on the symbol and graphically select the masked wells using the
well selection options and click OK. The selected wells are shown with a dashed border
around them. The coordinates of the selected masked wells are reported in the Selection
Note: When entering details into the fields, the mandatory fields will be displayed in red until
all have been completed.
Note: The well selection methods for defining masked wells are the same as used for selecting
wells in the plate layout. View the Well Selection section on the Creating and Modifying Plate
Layouts page for details.
4. Enter the required information into the plate geometry fields by either entering numbers into
the fields or using the field's arrows to increment the existing values. All fields must be
completed before the plate definition can be saved and used.
Plate Length: The total length of the plate
Plate Width: The total width of the plate
Plate Height: The total height of the plate
A1 Column Offset: The distance in the x direction from the edge of the plate to the
centre of well A1 (column one, row one)
A1 Row Offset: The distance in the y direction from the edge of the plate to the centre
of well A1 (column one, row one)
Column Spacing: The distance in the x direction between the centre of adjacent wells
Row Spacing: The distance in the y direction between the centre of adjacent wells
Well Diameter: The well diameter
The plate geometry schematic updates to reflect the values entered into the fields.
Note:All values are in millimetres and are displayed to two decimal places unless the plate
comprises 384 wells or more in which case the values are displayed to three decimal places .
Note: Each field has minimum and maximum limits.
Note: The Well Diameter parameter in the plate geometry section and Diameter at Top
parameter in the well geometry section correspond to the same physical parameter. The Plate
Height parameter in the plate geometry section imposes a maximum limit on the Depth
parameter in the well geometry section. This coupling can result in invalid entries in one section
effecting entries in the other section.
5. Enter the required information into the well geometry fields by either entering numbers into the
fields, using the field's arrows to increment the existing values or the drop down list. All
fields must be completed before the plate definition can be saved and used.
Well Bottom Profile: Select the profile from the options available in the drop down list
Diameter at Top: The diameter at the top of the well
Depth:The distance from the bottom to the top of the well
Diameter at Bottom: The diameter at the bottom of the well
Recommended Minimum Volume: The recommended minimum fill volume for each
well when taking measurements
Recommended Maximum Volume: The recommended maximum fill volume for each
well when taking measurements
Actual Maximum Volume: The maximum fill volume for each well
The well geometry schematic updates to reflect the values entered into the fields.
Note:All values are in millimetres and are displayed to two decimal places unless the plate
comprises 384 wells or more in which case the values are displayed to three decimal places .
Note: The well diameter field in the plate geometry section and diameter at top field in the well
geometry section correspond to the same physical parameter. This can result in invalid entries
in one section effecting entries in the other section.
6. Save the plate definition
Note: The modified plate definition cannot have the same name, or be saved with the same
name, as an existing plate definition.
See also:
o Saving and opening plate definitions
o Removing plate definitions from the database
3. View a plate definition that has been saved to the database. If necessary, open a plate
definition from the database
Note: If the plate definition cannot be removed from the database because a copy has not been
saved to the database, a warning dialog is displayed.
Note: If the plate definition cannot be removed from the database because it is used by a plate
layout that has been saved into the database, a warning dialog is displayed.
Galapagos provides tools to create plate layouts comprising single or multiple physical plates. Wells
can be grouped together by well type and multiple groups can be assigned across a plate layout.
Each plate layout tab can display a single plate layout, whether newly created or opened from a
previously saved layout. Additional plate layout tabs can be created by repeating Steps 1 & 2
above.
The Database and File groups enable plate layouts to be saved and previously saved layouts
opened
The Plates group enables the plate definition (the type of plate) to be selected and plates to be
added and removed to a plate layout
The Groups and Wells groups provides tools to organise wells into groups
Groups Tab
Click on the Groups tab to display the corresponding Groups pane. The Groups pane lists the
groups assigned to each plate on the plate layout and displays the name and description of
each.
By default, groups are named 'Group n' where n is a number and for the first group created is 1
and which is incremented by 1 for each subsequent group created. Group names can be edited
but have to be unique. Each group can be given an optional description.
To always show the pane, click on the pin symbol. A horizontal splitter bar in between the
Layout and Selected Group sections and Selected Groups and Selected Well sections enables
the layout of the pane to be customised.
To expand the plate definition category, click on the symbol. The reduce the plate definition
category, click on the symbol.
Note: If the plate layout is saved and the file name is not the same as the plate layout name,
Galapagos will automatically adjust the name to be the same as the file name.
The Selected Group section displays the properties of the group of currently selected wells.
o The name and description can be edited by clicking in the Name and Description edit
fields. The group name has to be unique.
o For each group, the well type has to be defined by selecting an option from the drop-
down list. The options are Sample, Reference, Control and Standard.
o The Seed is the prefix used to identify each well within the group. By default, the
seed takes the name of the Well Type. The seed can be edited by clicking in the Seed
edit field. The suffix is a number starting at 1 and incremented by 1 for each
additional well in the group.
o The number of wells in the group is reported. This field cannot be edited and is
therefore displayed in grey.
o The well locations of the group are reported using their coordinates in the main plate
layout display. The coordinates are reported row letter then column number. This field
cannot be edited and is therefore displayed in grey.
o The number of replicates is shown. By default, the number of replicates is set to a
value of 1. The value can be increased and decreased to an integer value between 1
and 10000, inclusive, by clicking on the arrows to adjust the current value or
typing directly into the edit field.
o The number of replicates can be set to equal the number of wells in a given group by
setting the field to be True. The default setting for all group types is True.
o The details of any constants applied to the group are shown. This field cannot be
edited and is therefore displayed in grey.
Note: The Seed and Selected Well Name can be returned to default values by deleting the
custom entry.
Note: When replicates are set, replicates are organised first by row and then by column. For
example, a group comprising 8 wells in locations A1, A2, A3, B1, B2, B3, C1 and C2 with
replicates set to 4 has wells A1, A2, A3 and B1 as one replicate set and B2, B3, C1 and C2 as a
replicate set.
To zoom in and out of the plate display, click on the symbol and symbol respectively.
Alternatively, click and drag the slider bar toward the symbol to zoom in
See Also:
o Saving and opening plate layouts
o Creating and modifying plate layouts
o Removing plate layouts from the database
Note:The layout name and file name must be the same. If the plate layout is saved and the file
name is not the same as the plate layout name, Galapagoswill automatically adjust the name to
be the same as the file name.
Note: The layout name must be unique. If an attempt is made to save the layout with the same
name as an existing layout an error message is displayed.
Select an existing plate definition from the database - clicking on this option will
prompt the selection of a plate definition from those existing in the database. The
options will be limited to those with the corresponding number of rows and columns.
Create a new plate definition from the details already assigned to the layout and save
to the database - clicking on this option will prompt for a plate definition name before
saving to the database.
Note: Plate layout files are saved with the file extension .layout
Note: The layout name must be unique. If an attempt is made to save the layout with the
same file name as an existing layout an error message is displayed.
4. Select the layout to be opened from the list displayed and click Open
The plate layout is displayed in the active tab in the plate layout display
Note: It is not possible to open data from an empty database. If attempted, a warning dialog is
displayed.
3. Select the layout to be opened from the list displayed and click Open
The plate layout is displayed in the active tab in the plate layout display
Note: If a plate layout is not stored in the database, a warning dialogue is displayed:
All plates in the plate layout will be of the type defined by the plate definition file.
4. The Properties tab will show the plate definition details in the Plate Definition entry in the
Layout section.
The entry can be expanded to show all plate parameters using the symbol and reduced to
hide the parameters using the symbol. The fields are read only and cannot be edited.
The group tab updates to show an entry for each plate with the groups assigned to each plate
detailed.
The watermark displayed on the plate indicate its plate number in the plate series
Note: If additional plates are added to the default layout, then the new plates will be created
comprising the same layout. If additional plates are added to a non-default layout, then the
new plates will be created with all wells assigned to a new group of samples wells.
Note: Wells from different plates can be assigned to belong to the same group.
Note: When reducing the number of plates in a layout, the most recently added plate is
removed.
Note: Groups that only appear on a plate which has been removed are deleted from the layout
all together.
The watermark displayed on the plate indicate its plate number in the plate series
Select the group of interest by clicking on the corresponding group name from those listed in
the Group tab
Selecting Wells:
1. To select a single well, click on the well of interest
The keyboard Control key enables well selection methods to be combined. With a well or
set of wells selected, press and hold the keyboard Control key before selecting the next
set of wells. Any combination of the above selection methods is permitted.
Note: Multiple well selection is confined to wells from the same plate. To configure a group to
comprise wells from more than one plate, see Adding Wells to Existing Groups.
Note: Wells on plates that have been assigned as masked wells during the plate's definition
cannot be selected. These masked wells are labelled N/A.
3. Click on Yes
Note: If default group naming is used, when a group is removed from the layout, the groups
using default naming are renumbered so the first of the remaining groups to be added to the
layout is called 'Group '1, the next 'Group 2' and so on.
2. Click on Yes
Note: The Clear Groups command removes all groups from all plates of the layout.
Name: By default, groups are named 'Group n' where n is a number and for the first group
created is 1 and which is incremented by 1 for each subsequent group created. Group names
can be edited by clicking in the name edit field but have to be unique
Description: By default, no description is provided. Click in the description edit field to enter a
description
Well Type: Each group must be assigned one of the four well types from the drop down list. By
default this is set to the Sample option
The border used to highlight the group is coloured according to the well type selected. The
colours are:
Sample: red
Reference: green
Control: blue
Standard: orange
To update the group's well assignment, click on button. This will update the plate layout
display to reflect the revised assignment.
Note: Name, description and well type can be modified using the plate layout property pane
Note: A well can be part of only one group
Note: Name, description and well type can be modified using the plate layout property pane
Note: A well can be part of only one group
Note: This operation can be performed on plate layouts which comprise multiple plates.
Note: To remove wells from a group that comprises wells from more than one plate, remove
the necessary wells from each plate separately.
2. If the existing plate layout has not been saved, a prompt will be displayed warning of possible
data loss. Click Yes to continue.
Note: A constant can only be added a an individual well if the well is part of a group.
4. Enter the name of the constant and, optionally a description, in the Name and Description edit
fields of the Add Constant dialogue
5. Select the type of constant to assign by selecting either Static or Prompted from the Type drop
down list
Note: A static constant always has the same value. The value of a prompted constant is
requested before it is used in a data manipulation.
If a Static constant has been selected, enter the value to be used in the Value edit field
Click OK
2. Select the constant to delete from the list displayed and click on OK
Note: By default, the number of replicates for a group is set to a value of one. The range of
valid values is one to ten.
Note: The replicates run in sequence through the wells.
Note: By default, the number of replicates for a group is set to a value of one. The range of
valid values is one to ten.
Note: The replicates run in sequence through the wells.
3. View a plate layout that has been saved to the database. If necessary, open a plate layout from
the database
4. Click on Remove from Database
Note: If the plate layout cannot be removed from the database because a copy has not been
saved to the database, a warning dialog is displayed.
Note: If the plate layout cannot be removed from the database because it is has been used
when taking a measurement, a warning dialog is displayed.
Select an item from the list below for further information on the presentation of measurement and
manipulation results:
o Detailed Well View
Note: Wells can be selected using the mouse and a single-click or by using the keyboard arrow
keys.
Well selection, results data (both measured and manipulated) and graphical data are shown
where relevant.
The layout of the view can be modified by dragging the vertical splitter located between the
results data and chart display sections. The cursor is located above the splitter when it is
displayed as an arrow.
Note: When displaying data comprising two or more cycles, the time stamp of the data in the
Results Data section is quoted as the time the data was acquired and is stated as HH:MM:SS
(hour of the day : minute of the hour : second of the minute).
3. To exit the detailed well view and return to the main results display, either press the keyboard
To Apply Manipulations:
1. Configure a Quick Measurement but do not start the measurement_Ref-1999240534
2. Click on the Manipulate tab
3. Define, save, edit and remove equation(s) to apply to the raw measurement data or the results
of previously manipulated data
4. Click on the Acquire tab from the Method Tools context group and click Start
The data window updates to show the measurement results. Each well can display a maximum
of three values and can be a combination of raw and manipulated data. Well data displayed in
bold corresponds to manipulated data, i.e. calculated values.
Where there is more than three data values (measured and manipulated data) for a well, only
the results of the data manipulations are displayed with the outcome of any screening equations
taking president over the results of other manipulation types. If there are more than three
manipulation results, only the last three of the sequence are displayed. Both raw and processed
data values can be displayed in the data view pane by selecting a well of interest. Double-
clicking on a well of interest displays the Detailed Well View which shows both raw and
manipulated results data.
Note: There is no limit to the number of manipulations that can be applied to the results
data.
Note: The Method Properties pane displays the details of any specified equations.
Note: The manipulations and the results of manipulations are stored together with the raw
measurement data and other properties when the file is saved.
To Apply Manipulations:
1. Open a previously saved results file
2. Define, save, edit and remove equation(s) to apply to the raw measurement data or the results
of previously manipulated data
3. Click on Perform Manipulation
The data window updates to show the measurement results. Each well can display a maximum
of three values and can be a combination of raw and manipulated data. Well data displayed in
bold corresponds to manipulated data, i.e. calculated values.
Where there is more than three data values (measured and manipulated data) for a well, only
the results of the data manipulations are displayed with the outcome of any screening equations
taking president over the results of other manipulation types. If there are more than three
manipulation results, only the last three of the sequence are displayed. Both raw and processed
data values can be displayed in the data view pane by selecting a well of interest. Double-
clicking on a well of interest displays the Detailed Well View which shows both raw and
manipulated results data.
Note: There is no limit to the number of manipulations that can be applied to the results
dataa.
Note: The Method Properties pane displays the details of any specified equations.
Note: The manipulations and the results of manipulations are stored together with the raw
measurement data and other properties when the file is saved.
Setting Equations
Manipulations are configured in Galapagos by defining equations that are applied to the measured
results data or to previously manipulated data sets. Manipulations can be applied to individual wells or
groups of wells.
The following topics are covered in this section:
o Available mathematical operations
o Applying a new equation
o Discarding an equation
o Editing an existing equation
o Removing an existing equation
o Removing all existing equations
o Changing the order of equations
Arithmetic:
o Addition
o Subtraction
o Multiplication
o Division
Functions:
o Power
o Natural log
o Log base 10
o ex
o 10x
Note: The power operator requires two inputs to be specified. The others within this category
only require a single operator to be specified.
Concentration:
o Concentration (note: Concentration = [Absorbance] x [Concentration Factor] x [Dilution Ratio]
x [Weight Correction])
Note: Concentration requires four inputs to be specified. Dilution Factor and Weight Correction
are defined as follows:
Dilution Factor = Aliquot Volume / (Aliquot Volume + Diluent Volume)
Weight Correction = Sample Weight / Nominal Weight
Note: For information on how to setup a quantitative analysis see Introduction to Quantitative
Analysis.
Note: The Quantitative Analysis operator is only available when the method includes a plate
layout with at least 2 standards present.
Note: The statistical group of operators are applicable to replicates only. They require a single
input to be specified.
Comparison:
o Greater than: >
o Greater or equal to: >=
o Less than: <
o Less than or equal to: <=
Screening:
o Screen
This operator is used to partition wells into different categories according to their value.
This operator is used to remove erroneous well results - outliers - from manipulations that affect the
Results Validity. Following removal of an outlier, the manipulations are recalculated using the
remaining wells. Outliers continue to be removed until either the Results Validity changes from Invalid
to Valid or the maximum number of specified outliers has been removed.
The criteria for selecting which well value to remove is the well value which is furthest from the mean
value. The maximum number of outliers that can be removed is configurable. Note that the Remove
Outlier operator must refer to a group for which the number of replicates and wells are equal.
Note: the Comparison manipulation types can be used to determine Results Validity.
4. For the first input to the equation, select either All, Group or Well from the displayed
list
If All was selected, click on the arrow displayed after the previous selection and
select the appropriate measurement wavelength and proceed to Step 5.
If Group or Well was selected, click on the arrow displayed after the previous
selection and either select the appropriate group or well from the displayed list of
options. The groups are referred to by their given group name. Only wells that are
part of a group can be selected
or
Click on the arrow displayed after the previous selection and either select the
appropriate measurement wavelength or result from an existing manipulation (if a
manipulation has been previously configured)
If All was selected, click on the arrow displayed after the previous selection and
select the appropriate measurement wavelength and proceed to Step 6.
If fixed has been selected, enter the required value into the edit field or use the
If group or well has been selected, click on the arrow displayed after the previous
selection and either select the appropriate group or well from the displayed list of
options. The groups are referred to by their given group name. Only wells that are
part of a group can be selected
or
Click on the arrow displayed after the previous selection and either select the
appropriate measurement wavelength. or if acting on a group a result from an
existing manipulation (if a manipulation has been previously configured) or a constant
that has been assigned to a well or group
This is not a mandatory entry. The default name will be applied if a custom name is
not specified. The equation name is used to reference the equation in the Method
Properties window and when selecting to remove or edit an equation
A validation error dialogue is displayed if the defined equation contains errors that
prevent it from executing on the data. The equation is not saved and requires
correction before saving can be attempted again
Note: There is no limit to the number of manipulations that can be applied to the
results data.
Note: Equations run sequentially in the order they are specified.
Functions:
1. From the Manipulate tab of the Method Tools context group, click on New Equation
4. For the first input to the equation, select either All, Group or Well from the displayed
list
If All was selected, click on the arrow displayed after the previous selection and
select the appropriate measurement wavelength and proceed to Step 5.
If Group or Well was selected, click on the arrow displayed after the previous
selection and either select the appropriate group or well from the displayed list of
options. The groups are referred to by their given group name. Only wells that are
part of a group can be selected
or
5. To define the second input for the power operator, select either All, Group, Wellor
Fixed from the displayed list
If All was selected, click on the arrow displayed after the previous selection and
select the appropriate measurement wavelength and proceed to Step 6.
If Fixed has been selected, enter the required value into the edit field or use the
If Group or Well was selected, click on the arrow displayed after the previous
selection and either select the appropriate group or well from the displayed list of
options. The groups are referred to by their given group name. Only wells that are
part of a group can be selected
or
Click on the arrow displayed after the previous selection and either select the
appropriate measurement wavelength or if acting on a group a result from an existing
manipulation (if a manipulation has been previously configured) or a constant that
has been assigned to a well or group
6. Enter a name for the equation in the edit field next to the equals symbol
This is not a mandatory entry. The default name will be applied if a custom name is
not specified. The equation name is used to reference the equation in the Method
Properties window and when selecting to remove or edit an equation.
A validation error dialogue is displayed if the defined equation contains errors that
prevent it from executing on the data. The equation is not saved and requires
correction before saving can be attempted again.
Note: There is no limit to the number of manipulations that can be applied to the
results data.
Note: Equations run sequentially in the order they are specified.
Concentration:
Concentration:
1. From the Manipulate tab of the Method Tools context group, click on New Equation
4. For the first (absorbance) input to the equation, select either All, Group or Well from
the displayed list
If All was selected, click on the arrow displayed after the previous selection and
select the appropriate measurement wavelength and proceed to Step 5.
If Group or Well was selected, click on the arrow displayed after the previous
selection and either select the appropriate group or well from the displayed list of
options. The groups are referred to by their given group name. Only wells that are
part of a group can be selected
or
Click on the arrow displayed after the previous selection and either select the
appropriate measurement wavelength or if acting on a group a result from an existing
manipulation (if a manipulation has been previously configured)
If fixed has been selected, enter the required value into the edit field or use the
If group or well was selected, click on the arrow displayed after the previous
selection and either select the appropriate group or well from the displayed list of
options. The groups are referred to by their given group name. Only wells that are
part of a group can be selected
or
Click on the arrow displayed after the previous selection and select the appropriate
constant that has been assigned to a well or group.
This is not a mandatory entry. The default name will be applied if a custom name is
not specified. The equation name is used to reference the equation in the Method
Properties window and when selecting to remove or edit an equation.
A validation error dialogue is displayed if the defined equation contains errors that
prevent it from executing on the data. The equation is not saved and requires
correction before saving can be attempted again.
Note: There is no limit to the number of manipulations that can be applied to the
results data.
Note: Equations run sequentially in the order they are specified.
Quantitative Analysis:
1. From the Manipulate tab of the Method Tools context group, click on New Equation
2. From the list displayed, select the Quantitative Analysis manipulation type
3. Using the equation editor that appears in the Equation group, select the inputs for the
equation by clicking on the arrows in the operand edit fields and selecting the
appropriate item from the prompted lists.
4. For the first (absorbance) input to the equation, select either All, Group or Well from
the displayed list
If All was selected, click on the arrow displayed after the previous selection and
select the appropriate measurement wavelength and proceed to Step 5.
If Group or Well was selected, click on the arrow displayed after the previous
selection and either select the appropriate group or well from the displayed list of
options. The groups are referred to by their given group name. Only wells that are
part of a group can be selected
or
Note: Only manipulations that are applicable to all wells (use the 'All' option in the
equation editor) can be referenced in the equation.
5. For the second (Quantitative Analysis) input select the QA object to use. Select QA
and then the choose the QA object from the list displayed
6. For both the third (dilution ratio) and fourth (weight correction) inputs to the
equation, select either Group or Fixed from the displayed list
If fixed has been selected, enter the required value into the edit field or use the
If group has been selected, click on the arrow displayed after the previous selection
and select the appropriate group from the displayed list of options. The groups are
referred to by their given group name.
Click on the arrow displayed after the previous selection and select the appropriate
standard concentration that has been assigned to the group.
Note: Standard concentrations are assigned to Standard groups through the plate
layout tools or the QA object tools.
7. Enter a name for the equation in the edit field next to the equals symbol
This is not a mandatory entry. The default name will be applied if a custom name is
not specified. The equation name is used to reference the equation in the Method
Properties window and when selecting to remove or edit an equation.
A validation error dialogue is displayed if the defined equation contains errors that
prevent it from executing on the data. The equation is not saved and requires
correction before saving can be attempted again.
Note: There is no limit to the number of manipulations that can be applied to the
results data.
Note: Equations run sequentially in the order they are specified.
Statistics:
Replicates are set through the Plate Properties tab.
1. From the Manipulate tab of the Method Tools context group, click on New Equation
4. For the input to the equation, select All or Group from the displayed list
If All was selected, click on the arrow displayed after the previous selection and
select the appropriate measurement wavelength and proceed to Step 5.
Note: When using the All option, the number of replicates is taken to be one and
the calculations are based on all the wells that are part of a group.
If Group was selected, click on the arrow displayed after the previous selection and
select the appropriate group. The groups are referred to by their given group name.
Click on the arrow displayed after the group name and either select the appropriate
measurement wavelength, a result from an existing manipulation (if a manipulation
has been previously configured) or constant that has been assigned to a group
5. Enter a name for the equation in the edit field next to the equals symbol
This is not a mandatory entry. The default name will be applied if a custom name is
not specified. The equation name is used to reference the equation in the Method
Properties window and when selecting to remove or edit an equation.
Note: There is no limit to the number of manipulations that can be applied to the
results data.
Note: Equations run sequentially in the order they are specified.
Note: The result of all statistical equations with the exception of deviation can be
used in other manipulations and applied to wells and groups of any type and size.
For this to be allowed, the number of replicates must be equal to the number of
wells in the group from which the statistics are calculated.
Note: The result of a manipulation involving the outcome of any statistical
equation (with the exception of deviation) and a fixed value can be used in other
manipulations and applied to wells and groups of any type and size. For this to be
allowed, the number of replicates must be equal to the number of wells in the
group from which the statistics are calculated. An example would be to obtain the
mean value from a group of wells, add a fixed value to this mean and the divide
the value of the wells in another group by this value.
Note: When the number of replicates is set to one, all wells in the group are
included in the calculation.
Note: The number of replicates can be set to be equal the number of wells in a
group through the Plate Properties tab.
Comparison:
1. From the Manipulate tab of the Method Tools context group, click on New Equation
4. For the first input to the equation, select either All, Group or Well from the displayed
list
If All was selected, click on the arrow displayed after the previous selection and
select the appropriate measurement wavelength and proceed to Step 5.
If Group or Well was selected, click on the arrow displayed after the previous
selection and either select the appropriate group or well from the displayed list of
options. The groups are referred to by their given group name. Only wells that are
part of a group can be selected
or
Click on the arrow displayed after the previous selection and either select the
appropriate measurement wavelength or if acting on a group, a result from an
existing manipulation (if a manipulation has been previously configured)
If All was selected, click on the arrow displayed after the previous selection and
select the appropriate measurement wavelength and proceed to Step 6
If fixed was selected, enter the required value into the edit field or use the arrows
to increment the existing value by a unit of 1 and proceed to Step 6
If group or well was selected, click on the arrow displayed after the previous
selection and either select the appropriate group or well from the displayed list of
options. The groups are referred to by their given group name. Only wells that are
part of a group can be selected
or
Click on the arrow displayed after the previous selection and either select the
appropriate measurement wavelength, constant assigned to a group or well, or, if
acting on a group, a result from an existing manipulation (if a manipulation has been
previously configured)
For the outcome of the comparison not to effect the results validity, select 'No effect
on result validity'
For the outcome of the comparison to effect the results validity and the results to be
invalid if the outcome of the comparison is True, select 'Results invalid if true'
For the outcome of the comparison to effect the results validity and the results to be
invalid if the outcome of the comparison is False, select 'Results invalid if false'
Note: The result validity is displayed in the Results section of the Method
Properties pane
8. Enter a name for the equation in the edit field next to the equals symbol
This is not a mandatory entry. The default name will be applied if a custom name is
not specified. The equation name is used to reference the equation in the Method
Properties window and when selecting to remove or edit an equation.
A validation error dialogue is displayed if the defined equation contains errors that
prevent it from executing on the data. The equation is not saved and requires
correction before saving can be attempted again.
Note: There is no limit to the number of manipulations that can be applied to the
results data.
Note: Equations run sequentially in the order they are specified.
Screen:
1. From the Manipulate tab of the Method Tools context group, click on New Equation
4. For the input to the equation, select either All, Group or Well from the displayed list
If All was selected, click on the arrow displayed after the previous selection and
select the appropriate measurement wavelength and proceed to Step 5.
If Group or Well was selected, click on the arrow displayed after the previous
selection and either select the appropriate group or well from the displayed list of
options. The groups are referred to by their given group name. Only wells that are
part of a group can be selected
or
Input the required number of categories into the Categories edit field by either typing
the required number into the edit field or using the arrows to increment the
existing value.
Define the data range limits for each of the categories by clicking on the arrow and
selecting either All, Group, Well or Fixed from the displayed list for each of the
required threshold levels.
If Group or Well has been selected, click on the arrow displayed after the previous
selection and either select the appropriate group or well from the displayed list of
options. The groups are referred to by their given group name. Only wells that are
part of a group can be selected
or
Click on the arrow displayed after the previous selection and either select the
appropriate measurement wavelength, a constant that has been assigned to a well or
a group or if acting on a group, a result from an existing manipulation (if a
manipulation has been previously configured)
Note: Values entered for the level threshold values must not be equal and be in
ascending order. A warning dialogue is displayed if the level thresholds are not in
ascending order.
6. Enter a name for the equation in the edit field next to the equals symbol
This is not a mandatory entry. The default name will be applied if a custom name is
not specified. The equation name is used to reference the equation in the Method
Properties window and when selecting to remove or edit an equation.
A validation error dialogue is displayed if the defined equation contains errors that
prevent it from executing on the data. The equation is not saved and requires
correction before saving can be attempted again.
Note: There is no limit to the number of manipulations that can be applied to the
results data.
Note: Equations run sequentially in the order they are specified.
4. For the input to the equation, select either Allor Group from the displayed list
If All was selected, click on the arrow displayed after the previous selection and
select the appropriate measurement wavelength and proceed to Step 5.
If Group was selected, click on the arrow displayed after the previous selection and
either select the appropriate group from the displayed list of options. The groups are
referred to by their given group name.
Click on the arrow displayed after the previous selection and either select the
appropriate measurement wavelength or a result from an existing manipulation (if a
manipulation has been previously configured)
5. Enter the number of proceeding equations that need recalculating after the outlier has
been removed
Note: Where more than one remove outlier equation is included in a sequence of
equations, the equation count for a given remove outlier equation cannot be set to
include another remove outlier equation.
Note: The minimum number of outliers will be removed to produce a valid results
validity. If this has not been achieved the maximum number of outliers has been
removed the routine will complete the results validity will remain invalid.
Note: After the remove outliers equation has completed, the wells that have been
removed are indicated with the label 'Excluded'.
This is not a mandatory entry. The default name will be applied if a custom name is
not specified. The equation name is used to reference the equation in the Method
Properties window and when selecting to remove or edit an equation.
A validation error dialogue is displayed if the defined equation contains errors that
prevent it from executing on the data. The equation is not saved and requires
correction before saving can be attempted again.
9. Additional Remove Outlier equations and other equations can be defined and set
Note: There is no limit to the number of manipulations that can be applied to the
results data.
Note: Equations run sequentially in the order they are specified.
To Discard an Equation:
1. To cancel either the process of defining a new equation or editing an existing equation, click on
Discard Equation from the Manipulate tab of the Method Tools context group
Note: The equation being edited is not removed from the saved list of equations.
3. Edit the equation as required using the equation editor in the Equations group of the ribbon
Note: The equation used to calculate the difference between the measurement and reference
values in dual wavelength mode cannot be edited.
3. Click Yes
Note: The equation used to calculate the difference between the measurement and reference
values in dual wavelength mode cannot be removed.
2. Click Yes
All equations are removed and are no longer part of the method
Note: The equation used to calculate the difference between the measurement and reference
values in dual wavelength mode cannot be removed.
4. Click OK
These tools enable quantitative analysis objects to be created, edited and the standard curve viewed.
Previously configured quantitative analysis objects can also be imported and validated. Quantitative
analysis objects comprise the details of which standards to analyse and how to analyse the standards
to create the standard curve. These are plots of concentration against measured absorbance.
Once a quantitative analysis object has been setup it can be used to calculate the concentration of
samples. This is performed by adding a manipulation that uses the Quantitative Analysis equation.
There are two parts to performing a quantitative analysis. These are:
1. Creating a Quick Measurement method that incorporates Quantitative Analysis
2. Performing a Quantitative Analysis to measure the concentration of samples
To Open a New Quick Measurement and Define a Plate Layout Incorporating Standards:
1. Click on the Methods tab and on Quick Measurement
3. Either Open from database or from file a previously saved plate layout that includes standard
groups
Or,
Note: A plate layout does not require standard groups if the quantitative analysis uses an
imported QA object See Importing QA Objects for more information.
Note: The number of standards defined by a standards group is given by the number of wells
divided by the number of replicates. By default, groups comprising standards are set to have
the number of replicates equal to the number of wells. Setup in this way, a standard group
comprises one standard for the purposes of the QA. Alternatively, by setting the number of
replicates to less than the number of wells within a group, the number of standards in the
group can be greater than one and up to a value equal to the number of wells in the group.
The minimum number of standards required to perform a quantitative analysis is determined by
the interpolation or fitting function specified when configuring a QA object. Some functions
require a minimum of two standards, others a minimum of six standards.
Note: When replicates are set, replicates are organised first by row and then by column. For
example, a group comprising 8 wells in locations A1, A2, A3, B1, B2, B3, C1 and C2 with
replicates set to 4 has wells A1, A2, A3 and B1 as one replicate set and B2, B3, C1 and C2 as a
replicate set.
From the displayed list, double-click on each standard in turn and enter the corresponding
name, description and concentration value and click OK
Note: The measurement mode and wavelength(s) must be compatible with the input to the QA
object(s) defined in Step 3 below.
Note: Only manipulations that are applicable to all wells (use the 'All' option in the equation
editor) can be used as an input.
Groups: Lists the standards groups that are used by the QA object. By default, all standard
groups are included. To modify which standard groups are used and the order of the groups:
Click Edit
Click Finished
Standards: Lists the details of the standards that have been defined. The Concentration field
for each standard can be used to edit the concentration value.
Extrapolated Range: Sets how far the standard curve is to be extended outside the range
of the standard concentrations. This option is only available for fitting functions. The
range is defined as a percentage of the concentration range and is applied to both the
low and high end of the standard curve.
Polynomial Order: Set the order of the polynomial. The value can be between 2 and 10
inclusive.
Click Close
6. Click on the Acquire tab, confirm the acquisition parameters and click on Start
Note: The plate display reports the measurement results, but no sample concentrations since
the manipulation using the Quantitative Analysis equation has not yet been set.
The upper pane shows the concentration - absorbance plot, the data points for each of the
standards and the corresponding standard curve.
The two tabular panes display the standard measurements & statistics and coefficient &
goodness of fit parameters. If all standards have a single replicate, the statistics columns are
not shown. The coefficient and goodness of fit parameters are not shown if the function selected
in the QA object is an interpolation.
If more than one QA object has been added, click on the Quantitative Analysis drop-down list to
select which QA object to display.
o To view the analysis of a different QA object (if more than one QA object has been
added):
o To change the x-axis type, click on the X-Axis Type drop down list and select either
Linear or Log:
Select the statistic type to display by checking the appropriate tick box. To select all
types, check the Column tick box.
o To change the standards and replicates that are included in the calculation of the
standard curve, select the required standards and replicates by checking the appropriate
tick boxes.
The standard curve updates to show only the standards that are included in the
calculation and the new line of best fit.
See also:
o Running a Quick Measurement method incorporating Quantitative Analysis
To Import a QA Object:
1. Click on the Method tab and click on Quick Measurement
If importing from the database, select the Quick Measurement results file or methods template
file and which quantitative analysis object to import and click on Import
4. Click on View Analysis to view the standard curve and related details
The upper pane shows the concentration - absorbance plot, the data points for each of the
standards and the corresponding standard curve.
To resize the area used to display each of the panes, move the mouse over the horizontal
and vertical splitters and drag to the required position.
o To view the analysis of a different QA object (if more than one QA object has been
added):
o To change the x-axis type, click on the X-Axis Type drop down list and select either
Linear or Log:
Select the statistic type to display by checking the appropriate tick box. To select all
types, check the Column tick box.
The standard curve updates to show only the standards that are included in the
calculation and the new line of best fit.
Note: When using an imported QA object, the plate layout does not have to include any
standard groups.
3. Either Open from database or from file a previously saved plate layout that includes standard
group(s)
Or,
Create a plate layout that includes standard group(s) and click on Accept Layout
Note: All standard groups must have the number of replicates equal to the number of wells.
4. Click on the Acquire tab and set the acquisition parameters to be compatible with the imported
QA object and click Start
Note: The measured data has to include the input to the QA object
The data for the standard is plotted on the standard curve and shown using a blue triangle.
The Measurement Offset is the y-axis offset from the new data point to the existing standard
curve
The Concentration Offset is the x-axis offset from the new data point to the existing
standard curve
The Calibration Offset is the same as the Measurement Offset
Note: The Method Properties pane updates to show in the Quantitative Analysis section the
validated QA object's settings
Note: When using an imported QA object, the plate layout does not have to include any
standard groups.
See Also:
o Creating a Quick Method Incorporating Quantitative Analysis
o Running a Quick Measurement method incorporating Quantitative Analysis
The concentration results for the QA manipulation are shown in bold for the sample group (the
two groups highlighted with a yellow border are standards groups).
The input values into the QA object for wells marked U/R and O/R are out of the range of the
standard curve. Concentration data cannot be calculated for these wells and they are labelled
under-range (U/R) and over-range (O/R) respectively.
6. Click in a well of interest to see well details in the Data pane
Exit the detailed well view and return to the main results display by either pressing the
The upper pane shows the concentration - absorbance plot, the data points for each of the
standards and the corresponding standard curve.
The two tabular panes display the standard measurements & statistics and coefficient &
goodness of fit parameters. If all standards have a single replicate, the statistics columns are
not shown. The coefficient and goodness of fit parameters are not shown if the function selected
in the QA object is an interpolation.
If more than one QA object has been added, click on the Quantitative Analysis drop-down list to
select which QA object to display.
o To view the analysis of a different QA object (if more than one QA object has been
added):
o To change the x-axis type, click on the X-Axis Type drop down list and select either
Linear or Log:
Select the statistic type to display by checking the appropriate tick box. To select all
types, check the Column tick box.
o To change the standards and replicates that are included in the calculation of the
standard curve, select the required standards and replicates by checking the appropriate
tick boxes.
The standard curve updates to show only the standards that are included in the
calculation and the new line of best fit.
See also:
o Creating a Quick Measurement Method Incorporating Quantitative Analysis
Report Writer
The report writer provides an integrated collection of tools to create and configure report templates
from which reports can be produced when combined with measurement, manipulated and instrument
data.
The following topics are covered in this section:
o Launching the report writer
o The components of the Report Designer tab
o Creating and editing a report template
Design surface:
The design surface is the area on to which report objects are placed, aligned and formatted and where
reports can be previewed.
The design surface tool bar provides the following viewing and alignment options:
Click on the Designer tab to show the design surface and manipulate the report
objects
Click on the Preview tab to preview the report (requires a data source to have been
set). See section below for more details.
Click on the Dimension Lines icon to display dimension lines when dragging objects around the
design surface that run from the borders of the report to the object
Click on the Hide Grid icon to hide the grid lines and dots on the design surface
Click on the Show Dots icon to show dots in between the grid lines on the design surface
Click on the Show Lines icon to show lines in between the grid lines on the design surface
Click on the Snap Lines icon to display snap lines when the object being dragged is aligned with
other objects on the design surface
Click on the Snap to Grid icon to restrict the placement of an object to coincide with the grid
lines when dragging an object around the design surface
Click on the Select Mode icon to set the cursor mode to allow object selection and alignment
Click on the Pan Mode icon to set the cursor mode to pan navigation
Drag the slider bar anchor or click on the minus and positive buttons
A data source is required to have been set for any report objects to report on measurement,
manipulated or instrument data. The entire data set can be reported on or filters can be set to limit
the data reported on to a subset of the whole data set.
Select which data channels to include in the report preview by checking the appropriate check box. A
tick denotes the data channel is selected for inclusion.
To view the preview based on the loaded data set and any applied data filters, click Refresh on
the Preview toolbar.
The Preview window displays the report and the toolbar provides numerous tools to aid viewing,
copying and printing.
Zoom Value Click on the arrow to select a zoom level or type the
required zoom level value in the edit field
Fit Width Click to adjust the display properties so the full width
of each page of the report is displayed
Fit Page Click to adjust the display properties so the each
page of the report is displayed in full
Single Page View Click to display a single page. To view other pages,
use the Page Controls (see below)
Continuous Page Click to view pages using the scroll bar to scroll
View through the pages or by using the Page Controls (see
below)
Page Controls Click on the arrows to view the first page, previous
page, next page and last page respectively
Backward Displays the last viewed page (once clicked, the
Forward button is enabled)
Forward Displays the last viewed page before the Backward
button was clicked
Pan Click to use pan navigation control
There is also an advanced approach to create and edit report templates. This is:
o Advanced Reporting-Using objects from the Page Reports pane
Report templates can be created and edited using any combination of these methods.
Report templates are combined with measurement, manipulated and instrument data to produce
reports.
Existing report templates can also be used into create new templates. The two approaches to
achieving this are:
o To open an existing report template, modify the content and layout and save as a new report
template
o To create a new (empty) report template and paste content into it by copying parts of existing
report templates
Together with using Data and Style Options, these methods fall into the category of standard
approaches to create report templates.
3. Open a previously saved report template by clicking on either Open from Database or Open
from File, selecting the template of interest and clicking OK or Open
To move existing content to a new location on the design surface, first select the object or
group of objects by dragging a selection box around an object or group of objects.
An alternatively method of selecting the object of interest is to click on the object in the
Report Explorer tree view. Then click on the group select symbol and drag to a new
location.
To delete an object or group of objects, first select the object or group of objects by
draging a selection box around an object or group of objects.
Then either press the keyboard Delete key or right mouse click on the group select
symbol and select Delete. A dialogue is displayed requesting confirmation to delete. Click
OK.
An alternative method of deleting an object is to click on the object in the Report Explorer
tree view, right mouse click and select Delete.
To modify the properties of an object, select the object of interest and then modify the
property of interest in the Object Properties pane.
To insert an image into the report template, right mouse click on Embedded Images in the
Report Explorer and click on Add Embedded Image
Select the required image from the Open File dialogue and click Open. The Report Explorer
pane updates to show the image file in the tree view below Embedded Images. Select the
image in the Report Explorer's tree view and drag on to the design surface as required.
To add content to the report template, use one of the following methods:
o Copying content from other report templates
o Adding Data and Style Options
o Adding report objects
From the list that appears, select the source as either From Database or From File
From the displayed dialogue, select the required results file and click OK or Open
The name of the loaded results file is displayed in the status bar
Note: Ensure that the selected data is compatible with the report template. Blank reports can
result from reporting on data sets that do not comprise the data types the report template is
set to report on.
The report preview is displayed using the measurement, manipulated and instrument data
specified in Step 6.
Note: If a new data set has been specified since the report was last previewed, click on the
Refresh icon to update the report preview.
Note: Undo the previous operation by pressing the keyboard Ctrl and Z keys together.
Note: Content that is linked to measurement, manipulated or instrument data cannot be
located in either the header or footer sections of the report template.
3. Open a previously saved report template from which to copy content by clicking on either Open
from Database or Open from File, selecting the template of interest and clicking OK or Open
5. Click on the report template window tab which includes content to be copied.
To select the content of interest, drag a selection box around the object or group of objects.
An alternatively method of selecting the object of interest is to click on the object in the Report
Explorer tree view. Then right mouse click on the group select symbol and select Copy
6. Click on the new report template window tab
Right mouse click in the section (header, body, footer) of the report the content is to be pasted
and select Paste
The content appears in the new report in the centre of the selected section. Move the content to
the required location on the design surface.
To open a different report template from which to copy content, repeat Steps 1-3.
7. Save the report template by clicking on either Save to Database or Save to File, entering the
required filename and clicking OK or Save
And from the list that appears, select either From Database or From File
From the displayed dialogue, select the required results file and click OK or Open
The name of the loaded results file is displayed in the status bar
9. Select which data channels to include in the report preview by checking the appropriate check
box. A tick denotes the data channel is selected for inclusion.
Select which wells to include in the report preview by clicking on the tree view nodes to show
the wells selected within each group. Select the groups and wells to include in the preview by
checking on the appropriate check boxes. A tick denotes the data channel is selected for
inclusion.
The report preview is displayed using the measurement, manipulated and instrument data
specified in Step 8.
Note: If a new data set has been specified since the report was last previewed, click on the
Refresh icon to update the report preview.
Note: Undo the previous operation by pressing the keyboard Ctrl and Z keys together.
3. From the dialogue that is displayed, select the report template to open from the list displayed
and click on OK
4. Click on Remove from Database
See also:
o Standard Reporting-Using Data Options and Style Options
o Advanced Reporting -Using Page Reports Objects
o Producing reports
Plate
A general purpose report layout suitable for single, dual and multiple wavelength data and time
cycling data with one or more wavelengths
Together with using existing report templates, this method fall into the category of standard
approaches to create report templates.
3. Either, open a previously saved report template by clicking on either Open from Database or
Open from File,selecting the template of interest and clicking OK or Open
or,
Start a new report by clicking on New Report
Data Options:
See section 'Available Data and Style Options' for details of the Data and Style Options
available.
To modify the properties of a Data or Style Option, select the Data or Style Option by
either dragging a selection box around the contents of the Data or Style Option or clicking
on the name of the Data or Style Option in the Report Explorer tree view.
For Data or Style Options comprising several elements, individual elements can be selected
in the same way as Data or Style Options.
Modify the property of interest in the Option Properties pane.
Then either press the keyboard Delete key or right mouse click on the group select
symbol and select Delete. A dialogue is displayed requesting confirmation to delete. Click
OK.
Alternatively, select the object in the Report Explorer, right mouse click and select Delete.
7. To add additional Data or Style Option to the report template, repeat Steps 4 and 5.
Note: The default names given to Data or Style Options, and any elements they comprise,
when added to the design surface are unique. If names are modified (to be more descriptive)
they must be unique. The object's name is modified by editing the Name field in the Design
section of the Object Property pane.
8. To add additional content to the report template, use one of the following methods:
o Copying content from other report templates
o Adding report objects
From the list that appears, select the source as either From Database or From File
From the displayed dialogue, select the required results file and click OK or Open
The name of the loaded results file is displayed in the status bar
Note: Ensure that the selected data is compatible with the report template. Blank reports can
result from reporting on data sets that do not comprise the data types the report template is
set to report on.
11. Select which data channels to include in the report preview by checking the appropriate check
box. A tick denotes the data channel is selected for inclusion.
The report preview is displayed using the measurement, manipulated and instrument data
specified in Step 10.
Note: Undo the previous operation by pressing the keyboard Ctrl and Z keys together.
Data Options:
o Equations: Contains details of all manipulations defined for the method
o Group Details: Shows the details of the plate layout
o Group Equation Result: Tabulates group equation results (a group equation is a manipulation
that sources data from more than one well in the group but produces a single outcome. This
also applies to any result of this type which is further manipulated by a single term).
o Group Result: Tabulates all well results for a given group
o Instrument Identification: Contains instrument specific details
o Layout: Shows the grouping of wells in the plate layout
o Layout Identification: Shows the name and description of the plate layout
o Method Identification: Contains method specific information
o Multiple Well Chart: Displays chart data (absorbance vs time and absorbance vs wavelength)
from more than one well
o Operator Identification: Contains the compounded name comprising the computer and operator
name associated with the result
o Parameter Settings: Contains the method settings associated with the method
o Plate Definition: Displays information relating to the plate definition used
o Plate Result: Shows the results for each well organised by plate and group
o Plate View: Shows the plate view as displayed after a measurement
o Result Header: Contains basic results information and shows the results validity flag
o Standards: Contains details of the Quantitative Analysis Options
o Well Details: Displays details of individual wells defined in the plate layout
o Well Result: Displays individual well data
Style Options:
o Current Date & Time: Displays the current PC date and time
o Line: Displays a configurable line
o Page Number (N of M): Shows page numbers
o Signature Box: Displays a signature box
o Textbox: Inserts a text box for adding user specified text
Either open or create a report template that includes the content from which to create the Data
or Style Option.
4. Right mouse click on the group select symbol and click on Copy.
5. Click on Data Option or Style Option
Click on Create New Data Option from Contents of the Clipboard or Create New Style
Option from Contents of the Clipboard
The Data or Style Option list is updated to include the new Data or Style Option
Note: Data and Style Options are stored as .control files in the ProgramData/Biochrom
Limited/Galapagos folder.
Note: Remove Data or Style Options by deleting the corresponding .control file using Windows
Explorer.
Note: Undo the previous operation by pressing the keyboard Ctrl and Z keys together.
See also:
o Standard Reporting-Using Existing Report Templates
o Advanced reporting-Using Page Reports Options
o Producing reports
Data Options:
Equations: Contains details of all manipulations defined for the method
Group Equation Result: Tabulates group equation results (a group equation is a manipulation that
sources data from more than one well in the group but produces a single outcome. This also applies to
any result of this type which is further manipulated by a single term).
Multiple Well Chart: Displays chart data (absorbance vs time and absorbance vs wavelength) from
more than one well
Operator Identification: Contains the compounded name comprising the computer and operator
name associated with the result
3. Either, open a previously saved report template by clicking on either Open from Database or
Open from File, selecting the template of interest and clicking OK or Open
or,
start a new report by clicking on New Report
From the Page Reports pane, select and drag the required object type in to place on the design
surface
5. Configure the object's properties and/or measurement, manipulated & instrument data binding
settings
For details of how to configure the different Page Reports objects, see topic Setup of Page
Reports Objects
Note: Undo the previous operation by pressing the keyboard Ctrl and Z keys together.
7. To add additional content to the report template, use either of the standard methods:
o Copying content from other report templates
o Using Data and Style Objects
From the list that appears, select the source as either From Database or From File
From the displayed dialogue, select the required results file and click OK or Open
The name of the loaded results file is displayed in the status bar
Note: Ensure that the selected data is compatible with the report template. Blank reports can
result from reporting on data sets that do not comprise the data types the report template is
set to report on.
Select which wells to include in the report preview by clicking on the tree view nodes to show
the wells selected within each group. Select the groups and wells to include in the preview by
checking on the appropriate check boxes. A tick denotes the data channel is selected for
inclusion.
The report preview is displayed using the measurement, manipulated and instrument data
specified in Step 9.
Note: Undo the previous operation by pressing the keyboard Ctrl and Z keys together.
2. Press the keyboard Delete key or right mouse click on the group select symbol and select
Delete. A dialogue is displayed requesting confirmation to delete. Click OK.
2. Move the object to a new location on the design surface by clicking on the object's group select
symbol and either dragging the object to the required position or use the keyboard cursor
keys to move the object to the required position
Clicking on the tree view nodes expands each of these groups to show the data that can be reported
on:
Equation: The name and description of user-specified manipulations that directly manipulate
well results to create a manipulated well result
Equation (Group): The details of user-specified manipulations that produce a single result from
a group of wells
The common values available for reports are listed in the Report Explorer in the Common Values
folder:
To Configure Objects that can Report on Measurement, Manipulated and Instrument Data:
Certain Page Reports objects can be combined with data sources to report on measurement,
manipulated and instrument data and with common values such as page numbers and time & date.
Of the Page Reports objects described above, the following can be configured to report on results
data:
o BandedList
o Table
o Matrix
o Chart
BandedList:
A BandedList is used for creating lists of results types such as the Instrument group (name,
serial number and firmware version) or the Method group. It is also used for handling data
sources that have multiple values.
A BandedList comprises three sections - header, footer and central sections.
To add a data source or common value to a section of the BandedList, select the data source of
interest from the Report Explorer and drag in to the required section. More than one data
source or common value can be added, but results sources have to be from the same results
type, such as from the Instrument group or from the Plate group.
To add additional freehand text, select TextBox from the Page reports pane, drag into the
required section and edit the text box with the required text.
Example 1:
An example use of a BandedList is to list the instrument details. To do this:
1. Drag a Bandedlist onto the design surface
2. From the Page Reports pane, drag three TextBoxes into the central section of the
BandedList and arrange them one above the other on the left hand side
3. From the Report Explorer, drag the Name, Serial Number and Firmware Version fields
of the Instrument group into the central section of the BandedList. Arrange them one
above the other on the right hand side and aligned with the Textboxes on the left
4. Type an appropriate label into each of the Textboxes (Name, SN, FW Version)
5. From the Page Reports pane, drag another TextBox into the header section of the
BandedList, align it with the other Textboxes on the left hand side and type a title
(Instrument Settings)
Example 2:
An example use of a BandedList is to show the plate view. To do this:
1. From the Page Reports pane drag a BandedList on to the design surface
2. From the Page Reports pane drag an Image into the main section of the BandedList
3. Select the Image object and click on the results Selector icon, click on Plate
Image and then click on Image
4. Select the Image object and from the Data section of the Properties pane change the
Source field to 'Database' from the list of options
5. Select the BandedList and Image objects and resize as required
Note: Adjust the size of objects to meet the report requirements by selecting the object and
dragging the perimeter markers accordingly.
Note: All objects on the design surface must have a unique name. The object's name is
modified by editing the Name field in the Design section of the object's property pane.
Note: A data source must be set to preview the report.
Table:
A Table is used to show data in rows. The number of rows in a table varies with the data
source, but unlike a Matrix, the number of columns is fixed during the design process.
A table comprises three columns and three rows by default. The top row is the header section
used for column headings. The bottom row is the footer section. Text can be entered into these
cells as required or left blank if not required. Drag the required data sources into the middle
row. These can include items from the Data group.
More columns and rows can be added to a table. To add a row, click on the object, right mouse
click on the far left of the object and select either Insert Row Above or Insert Row Below. To
add a column, click on the object, right mouse click on the top of the object and select either
Insert Column to the Left or Insert Column to the Right.
Note: Only the first measured absorbance value can be reported in a table. Use a Matrix to
report on more than one absorbance value and any manipulated data.
Note: Adjust the size of objects to meet the report requirements by selecting the object and
dragging the perimeter markers accordingly.
Note: All objects on the design surface must have a unique name. The object's name is
modified by editing the Name field in the Design section of the object's property pane.
Note: A data source must be set to preview the report.
Matrix:
A Matrix is used for creating a grid of data where the number of row and columns can vary
according to the data set. This object is well suited to displaying fields from the Data group
where the Value field varies with one or more of the other Data fields such as Well or Cycle.
A Matrix comprises two columns and rows by default. The top left cell can be left blank or text
can be input to act as a label. The bottom left cell is the row header and the top right cell is the
column header. Drag the required Data fields into these cells. The bottom right cell is used to
display the value of the intersection of columns and rows.
More columns and rows can be added by clicking on the object and right mouse clicking on the
far left or top of the object, selecting Add Column Group or Add Row Group and clicking OK on
the dialogue that appears.
Example:
Another example use of a Matrix would be to display how the measured absorption value and
manipulated absorption value varied within each well and by cycle. To do this:
1. From the Page reports, drag a Matrix on to the design surface and create an
additional row group
2. Drag the Cycle field from the Data group into the bottom left cell, drag the Well field
from the Data group into the bottom centre cell, drag the Name field from the Data
group into the top right cell and drag the Value field from the Data group into the
bottom right cell
3. Select the bottom right cell and in the Properties pane edit the Value field in the Data
section to remove 'Sum' after the equals sign
If the data set selected to report on includes more than one measured wavelength or one or
more manipulations then these values will also be displayed.
Note: All measured and manipulated data channels can be reported in a Matrix.
Note: Adjust the size of objects to meet the report requirements by selecting the object and
dragging the perimeter markers accordingly.
Note: All objects on the design surface must have a unique name. The object's name is
modified by editing the Name field in the Design section of the object's property pane.
Note: A data source must be set to preview the report.
Example:
An example use of a Chart would be to plot how the absorbance varies with wavelength for a
series of wells. To do this:
1. From the Page Reports pane drag a Chart on to the design surface and select Line
2. Click on the chart and from the Reports Explorer drag the Value field from the Data
group into the region above the plot (region entitled: Drop data fields here), drag the
Name field from the Data group into the region below the plot (region entitled: Drop
category fields here) and drag the Well field from the Data group into the region to
the side of the plot (region entitled: Optionally drop series fields here)
3. Click twice on the chart and right mouse click over Value in the top left corner and
select Edit. In the dialogue that is displayed, edit the Value field by removing 'Sum'
after the equals sign and click OK
4. To edit the axis labels and chart title, select the default label on the chart and edit the
name in the Properties pane
Note: All objects on the design surface must have a unique name. The object's name is
modified by editing the Name field in the Design section of the object's property pane.
Note: A data source must be set to preview the report.
Image:
The Image object enables images to be displayed.
1. Right mouse click on Embedded Images in the Report Explorer and click on Add Embedded
Image. Using the displayed dialogue, browse and select the require image file.
2. Drag an image object on to the design surface
3. Select the image object on the design surface and through the Object Properties pane change
the Source field within the Data section to Embedded and select the name of the image
previously embedded in the Value field within the Data section.
Line:
The Line object allows straight lines to be displayed.
1. Drag a line on to the design surface
2. Each end of the line can be move to a new location on the design surface by selecting the line
and dragging each end to the required location.
3. Line styles are configured through the Object properties pane.
Shape:
The Shape object allows rectangles, circles and ellipses to be displayed.
1. Drag a shape on to the design surface
2. Adjust the size of the shape to meet the report requirements by selecting the object and
dragging the perimeter markers accordingly.
3. Change the shape through the Object Properties pane by selecting the required shape from the
ShapeStyle field in the Appearance section.
Note: All objects on the design surface must have a unique name. The object's name is
modified by editing the Name field in the Design section of the object's property pane.
To edit an object's properties, select the object and then edit the required fields displayed in the
Object Properties pane.
All objects on the design surface must have a unique name. The object's name is modified by editing
the Name field in the Design section of the object's property pane.
See also:
o Standard Reporting-Using existing report templates
o Standard Reporting-Using Data Options and Style Options
o Producing reports
Note: Where there is more than one data window open, the report takes data from the active
data window.
6. The Configure Reports dialogue updates to show the selected report template. Repeat steps 4
and 5 to add additional report templates to the Configure Reports dialogue.
Click OK to load the listed reported templates.
Note: Report templates only require loading into Galapagos once. On restarting the software,
previously loaded report templates are available to open.
The report template is opened and ready for use. The Select Data and Select Well filters update
accordingly.
2. Select which wells to include in the report by clicking on the tree view nodes to show the
wells selected within each group. Select the groups and wells to include in the report by
checking on the appropriate check boxes. A tick denotes the data channel is selected for
inclusion.
1. To view the report based on the loaded data set and any applied data filters, click Refresh
on the Report Viewer toolbar.
The Report Viewer updates to display the report
Zoom Value Click on the arrow to select a zoom level or type the
required zoom level value in the edit field
Fit Width Click to adjust the display properties so the full width
of each page of the report is displayed
Fit Page Click to adjust the display properties so the each page
of the report is displayed in full
Single Page View Click to display a single page. To view other pages,
use the Page Controls (see below)
Continuous Page Click to view pages using the scroll bar to scroll
View through the pages or by using the Page Controls (see
below)
Page Controls Click on the arrows to view the first page, previous
page, next page and last page respectively
Backward Displays the last viewed page (once clicked, the
Forward button is enabled)
Forward Displays the last viewed page before the Backward
button was clicked
Pan Click to use pan navigation control