Raw statistics for SNP dataset number 3 (settings -m 8 –N 2 –M 4 –n 3 -t). This dataset required SNPs to occur in 90% of individuals across 3 populations before being calle
<p>The call rates of SNPs (A) were first revealed among 55 samples after our hard filtering. The per...
<p>Number of SNPs detected in the WTCCC Breast Cancer dataset with Mutual Information Method and a t...
<p><i>N</i><sub>SNP</sub> – number of individuals included in the pools and number of technical repl...
Raw statistics for SNP dataset number 3 (settings -m 8 –N 2 –M 4 –n 3 -t). This dataset required SNP...
parameters set -m 8 –N 2 –M 4 –n 3 -t. This dataset required SNP occur across all populations at any...
parameters set -m 8 –N 2 –M 4 –n 3 -t. A filtered version of this dataset was used in analysis in pa...
Contains the SNP datasets used for analysis of genotyping error rates from reference alignment, refe...
Number of variants and genotyping rates for SNP datasets generated in this study.</p
13,912 SNPs called in 50% of 69 individuals with no less than 95% missing data, minimum stack depth ...
A) Single major allele calls; B) Double allele calls (DACs); C) Single minor allele calls; D) Missin...
<p>For the simulated datasets developed from 3-SNP models, average fraction over all 100 datasets of...
SNP dataset from GS reference mapper software: contig number, SNP position, reference and variant al...
A) Single major allele calls; B) Double allele calls (DACs); C) Single minor allele calls; D) Missin...
Genotype data for all 3,192 SNP loci (i.e., SNPs after filters, see manuscript for details) and all ...
<p>Summary of the common SNPs among eleven populations, the mean total SNP pairs (±Sd) within 10Mb a...
<p>The call rates of SNPs (A) were first revealed among 55 samples after our hard filtering. The per...
<p>Number of SNPs detected in the WTCCC Breast Cancer dataset with Mutual Information Method and a t...
<p><i>N</i><sub>SNP</sub> – number of individuals included in the pools and number of technical repl...
Raw statistics for SNP dataset number 3 (settings -m 8 –N 2 –M 4 –n 3 -t). This dataset required SNP...
parameters set -m 8 –N 2 –M 4 –n 3 -t. This dataset required SNP occur across all populations at any...
parameters set -m 8 –N 2 –M 4 –n 3 -t. A filtered version of this dataset was used in analysis in pa...
Contains the SNP datasets used for analysis of genotyping error rates from reference alignment, refe...
Number of variants and genotyping rates for SNP datasets generated in this study.</p
13,912 SNPs called in 50% of 69 individuals with no less than 95% missing data, minimum stack depth ...
A) Single major allele calls; B) Double allele calls (DACs); C) Single minor allele calls; D) Missin...
<p>For the simulated datasets developed from 3-SNP models, average fraction over all 100 datasets of...
SNP dataset from GS reference mapper software: contig number, SNP position, reference and variant al...
A) Single major allele calls; B) Double allele calls (DACs); C) Single minor allele calls; D) Missin...
Genotype data for all 3,192 SNP loci (i.e., SNPs after filters, see manuscript for details) and all ...
<p>Summary of the common SNPs among eleven populations, the mean total SNP pairs (±Sd) within 10Mb a...
<p>The call rates of SNPs (A) were first revealed among 55 samples after our hard filtering. The per...
<p>Number of SNPs detected in the WTCCC Breast Cancer dataset with Mutual Information Method and a t...
<p><i>N</i><sub>SNP</sub> – number of individuals included in the pools and number of technical repl...
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