<p><b>A)</b> Histogram of estimated log enrichment statistic, defined as the log of the bias corrected odds ratio comparing the allele frequency in AJ population to the maximum allele frequency estimated from NFE, AFR, and AMR populations in ExAC. For each histogram bin we show a bar plot of the expected number of alleles belonging to the two groups we analyzed: 1) enriched (green) and 2) not enriched (white). <b>B)</b> Bar plots of estimated percentage of alleles belonging to the two groups we analyzed for all protein-coding (ALL), synonymous (SYN), protein-altering (PRA), and protein-truncating variants (PTV). An estimate of 34% of protein-coding alleles observed in AJ have a mean shift of 15-fold increased odds of the alternate allele co...
Targeted capture combined with massively parallel exome sequencing is a promising approach to identi...
<p>Recalculation of the Supplementary Table 2 (doi:10.1371/journal.pcbi.1004647.s002) of the journal...
Motivation: In sequencing studies of common diseases and quantitative traits, power to test rare and...
Summary Large-scale reference data sets of human genetic variation are critical for the medical and ...
Large-scale reference data sets of human genetic variation are critical for the medical and function...
The dispensability of individual genes for viability has interested generations of geneticists. For ...
<p>The boxes span the lower and upper quartile with the median indicated by a red bar; whiskers exte...
Genetic studies have shifted to sequencing-based rare variants discovery after decades of success in...
To measure the strength of natural selection that acts upon single nucleotide variants (SNVs) in a s...
<p>(A) The distribution of the number of predicted exon-skipping ISE SNPs observed for each of the 1...
Computational tools are widely used for interpreting variants detected in sequencing projects. The c...
<p>Average number of variants remaining per sample after sequential or aggregate filtering steps.</p...
Over the past fifty years, the genetic bases for many human diseases have been discovered. Genome-wi...
Motivation: In sequencing studies of common diseases and quantitative traits, power to test rare and...
To measure the strength of natural selection that acts upon single nucleotide variants (SNVs) in a s...
Targeted capture combined with massively parallel exome sequencing is a promising approach to identi...
<p>Recalculation of the Supplementary Table 2 (doi:10.1371/journal.pcbi.1004647.s002) of the journal...
Motivation: In sequencing studies of common diseases and quantitative traits, power to test rare and...
Summary Large-scale reference data sets of human genetic variation are critical for the medical and ...
Large-scale reference data sets of human genetic variation are critical for the medical and function...
The dispensability of individual genes for viability has interested generations of geneticists. For ...
<p>The boxes span the lower and upper quartile with the median indicated by a red bar; whiskers exte...
Genetic studies have shifted to sequencing-based rare variants discovery after decades of success in...
To measure the strength of natural selection that acts upon single nucleotide variants (SNVs) in a s...
<p>(A) The distribution of the number of predicted exon-skipping ISE SNPs observed for each of the 1...
Computational tools are widely used for interpreting variants detected in sequencing projects. The c...
<p>Average number of variants remaining per sample after sequential or aggregate filtering steps.</p...
Over the past fifty years, the genetic bases for many human diseases have been discovered. Genome-wi...
Motivation: In sequencing studies of common diseases and quantitative traits, power to test rare and...
To measure the strength of natural selection that acts upon single nucleotide variants (SNVs) in a s...
Targeted capture combined with massively parallel exome sequencing is a promising approach to identi...
<p>Recalculation of the Supplementary Table 2 (doi:10.1371/journal.pcbi.1004647.s002) of the journal...
Motivation: In sequencing studies of common diseases and quantitative traits, power to test rare and...