<p>Columns report: library/lane identity (population A or B, estimation of sequencing depth per individual in Pool-seq, and software used to detect SNPs of Pool-seq data set), number of SNPs detected by GBS (SNP<sub>GBS</sub>) and Pool-seq (SNP<sub>Pool-seq</sub>), overlapping number of SNPs detected (SNP<sub>both</sub>), concordance correlation coefficient (CCC) with lower and upper 95% confidence limit (LCL; UCL) of CCC, the mean of the absolute difference in SNP frequency estimates of the two methods (|Δf|), false negative rate (FN rate), that is, the fraction of SNPs called by GBS but not by Pool-seq, and their mean minor allele frequency (FN MAF).</p
<p>The number in a cell means the number of SNPs with significantly different frequencies (with mult...
Several groups have developed methods for estimating allele frequencies in DNA pools as a fast and c...
<p>(<b>a</b>) The average percentage of missing data per SNP in each sequenced sample is plotted as ...
<p>Mean CCC values with upper and lower 95% confidence ranges are shown. The name of a library/lane ...
<p>The grey bars represent the SNPs present only in GBS. The striped bars represent the SNPs sequenc...
Population genomics is a fast-developing discipline with promising applications in a growing number ...
<p>The upper panel (dark grey) shows distributions when SNPs were called with VarScan for Pool-seq, ...
<p>The call rates of SNPs (A) were first revealed among 55 samples after our hard filtering. The per...
Sequencing pools of individuals (Pool-Seq) is a cost-effective method to determine genome-wide allel...
We have compared the accuracy, efficiency and robustness of three methods of genotyping single nucle...
Popoolation output file containing the read count data for polymorphic sites. The first column is th...
[Background]: Performing high throughput sequencing on samples pooled from different individuals is ...
a<p>: individual number was adapted from <a href="http://www.plosone.org/article/info:doi/10.1371/jo...
Association studies using DNA pools are in principle powerful and efficient to detect association be...
Background: Performing high throughput sequencing on samples pooled from different individuals is a ...
<p>The number in a cell means the number of SNPs with significantly different frequencies (with mult...
Several groups have developed methods for estimating allele frequencies in DNA pools as a fast and c...
<p>(<b>a</b>) The average percentage of missing data per SNP in each sequenced sample is plotted as ...
<p>Mean CCC values with upper and lower 95% confidence ranges are shown. The name of a library/lane ...
<p>The grey bars represent the SNPs present only in GBS. The striped bars represent the SNPs sequenc...
Population genomics is a fast-developing discipline with promising applications in a growing number ...
<p>The upper panel (dark grey) shows distributions when SNPs were called with VarScan for Pool-seq, ...
<p>The call rates of SNPs (A) were first revealed among 55 samples after our hard filtering. The per...
Sequencing pools of individuals (Pool-Seq) is a cost-effective method to determine genome-wide allel...
We have compared the accuracy, efficiency and robustness of three methods of genotyping single nucle...
Popoolation output file containing the read count data for polymorphic sites. The first column is th...
[Background]: Performing high throughput sequencing on samples pooled from different individuals is ...
a<p>: individual number was adapted from <a href="http://www.plosone.org/article/info:doi/10.1371/jo...
Association studies using DNA pools are in principle powerful and efficient to detect association be...
Background: Performing high throughput sequencing on samples pooled from different individuals is a ...
<p>The number in a cell means the number of SNPs with significantly different frequencies (with mult...
Several groups have developed methods for estimating allele frequencies in DNA pools as a fast and c...
<p>(<b>a</b>) The average percentage of missing data per SNP in each sequenced sample is plotted as ...