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  • Chromosome Original Number Mehods - Step1 - Number Mehods - Step2 - Number

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    Duc Nguyen Trung
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    A genome-wide association study (GWAS) is an approach used in genetics research to associate specific genetic variations with particular diseases. The method involves scanning the genomes from many different people and looking for genetic markers that can be used to predict the presence of a disease.A genome-wide association study (GWAS) is an approach used in genetics research to associate specific genetic variations with particular diseases. The method involves scanning the genomes from many d

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    Supplementary Table 11

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    A genome-wide association study (GWAS) is an approach used in genetics research to associate specific genetic variations with particular diseases. The method involves scanning the genomes from many different people and looking for genetic markers that can be used to predict the presence of a disease.A genome-wide association study (GWAS) is an approach used in genetics research to associate specific genetic variations with particular diseases. The method involves scanning the genomes from many d

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    Chromosome Original Number Mehods - Step1 - Number Mehods - Step2 - Number

    Uploaded by

    Duc Nguyen Trung
    A genome-wide association study (GWAS) is an approach used in genetics research to associate specific genetic variations with particular diseases. The method involves scanning the genomes from many different people and looking for genetic markers that can be used to predict the presence of a disease.A genome-wide association study (GWAS) is an approach used in genetics research to associate specific genetic variations with particular diseases. The method involves scanning the genomes from many d

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    © All Rights Reserved
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    of 2

    Supplementary Table 11 The summary of genome-wide SNP data used in the present study.

    Chromosome Original number Mehods_step1_number Mehods_step2_number


    chr1 1,946,047 1,754,807 465,501
    chr2 1,485,711 1,352,216 163,760
    chr3 1,452,223 1,312,696 391,580
    chr4 1,521,219 1,395,684 275,048
    chr5 1,241,765 1,121,062 276,395
    chr6 1,024,125 922,817 194,180
    chr7 1,107,288 1,003,206 250,024
    chr8 1,061,455 971,436 242,872
    chr9 974,605 885,136 258,699
    chr10 935,118 860,980 150,803
    total 12,749,556 11,580,040 2,668,862
    Mehods_step1: filtering heterozygous or missing genotype in any of two testers.
    Mehods_step2: only SNPs that had three genotypes (two homozygotes and one heterozygote)
    and minor genotypic frequency beyond 0.03 were retained.
    t study.

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