Publication date
September 2016
DOIAbstract
<p>Each cell count is the number of alleles in the sample collapsed from <a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0162910#pone.0162910.t001" target="_blank">Table 1</a>.</p
<p>Each cell count is the number of alleles in the sample collapsed from <a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0162910#pone.0162910.t001" target="_blank">Table 1</a>.</p
<p> indicates the number of SNP markers used in the model being evaluated. All other values indicate...
Popoolation output file containing the read count data for polymorphic sites. The first column is th...
The file contains the genotypes of all 948 individuals studied. Each row represents one individual.T...
<p>Codes of populations correspond to those of <a href="http://www.plosone.org/article/info:doi/10.1...
<p>Note: *No. of sample was in accord with no. of sample in <a href="http://www.plosone.org/article/...
<p>The complete list of sample ID, SNPs, miRNAs, and gene targets with more than one SNP is given in...
a<p>Number of alleles for each SNP is given in parentheses.</p>b<p>Significant <i>P</i> value (<0.05...
<p>For population codes see <a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.00...
<p>The table defines the mathematical notation for the recessive model for the M allele in the <a hr...
<p>Common haplotypes and estimated haplotype frequencies as determined using Haploview across the re...
<p>This figure displays the number of SNPs called for each of the 8 methods used. The proportion of ...
As explained in the Methods, only samples with all SNP successfully genotyped were included in the a...
This zipped file contains the number of reads matching each of two alternative allels for each indvi...
<p>Under each group label, left columns demonstrate the number of subjects for each genotype and all...
<p>Allele load (0,1,2) refers to the number of risk alleles: <i>677T</i> for <i>MTHFR C677T</i> and ...
<p> indicates the number of SNP markers used in the model being evaluated. All other values indicate...
Popoolation output file containing the read count data for polymorphic sites. The first column is th...
The file contains the genotypes of all 948 individuals studied. Each row represents one individual.T...
<p>Codes of populations correspond to those of <a href="http://www.plosone.org/article/info:doi/10.1...
<p>Note: *No. of sample was in accord with no. of sample in <a href="http://www.plosone.org/article/...
<p>The complete list of sample ID, SNPs, miRNAs, and gene targets with more than one SNP is given in...
a<p>Number of alleles for each SNP is given in parentheses.</p>b<p>Significant <i>P</i> value (<0.05...
<p>For population codes see <a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.00...
<p>The table defines the mathematical notation for the recessive model for the M allele in the <a hr...
<p>Common haplotypes and estimated haplotype frequencies as determined using Haploview across the re...
<p>This figure displays the number of SNPs called for each of the 8 methods used. The proportion of ...
As explained in the Methods, only samples with all SNP successfully genotyped were included in the a...
This zipped file contains the number of reads matching each of two alternative allels for each indvi...
<p>Under each group label, left columns demonstrate the number of subjects for each genotype and all...
<p>Allele load (0,1,2) refers to the number of risk alleles: <i>677T</i> for <i>MTHFR C677T</i> and ...
<p> indicates the number of SNP markers used in the model being evaluated. All other values indicate...
Popoolation output file containing the read count data for polymorphic sites. The first column is th...
The file contains the genotypes of all 948 individuals studied. Each row represents one individual.T...
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