The final product of our variant calling pipeline; obtained as described under: "Variant calling, filtering, and genotype refinement" in Supplementary Methods. This file includes both SNPs and indels. High coverage (15x) Massoko littoral and benthic samples are denoted by "HC" in sample names
Deficient homozygosity of a variant maintained in a population suggests that the variant may be embr...
Deficient homozygosity of a variant maintained in a population suggests that the variant may be emb...
Standardized benchmarking approaches are required to assess the accuracy of variants called from seq...
The final product of our variant calling pipeline; obtained as described under: "Variant calling, fi...
Motivation: Whole-genome high-coverage sequencing has been widely used for personal and cancer genom...
<p>Presentation at Genome Informatics 2013:</p> <p> </p> <p>Translational research relies on accurat...
Whole Exome Sequencing (WES) is used for querying DNA variants using the protein coding parts of gen...
abstract: Analyzing human DNA sequence data allows researchers to identify variants associated with ...
Discovery of genome-wide variation has taken a huge leap forward with the introduction of next-gener...
Improvement of variant calling in next-generation sequence data requires a comprehensive, genome-wid...
<p>Variant calling data from whole-genome sequencing of the Jurkat cell line. The data set includes ...
Summary of the variants called across the four resequenced Norwich Terriers using Platypus within th...
<p>Results from variant calling in the three workflows MiSEQ Reporter 2.1.43 (GATK variant caller), ...
<div><p>A diversity of tools is available for identification of variants from genome sequence data. ...
PEMapper and PECaller are paired software programs that simplify mapping and variant calling for who...
Deficient homozygosity of a variant maintained in a population suggests that the variant may be embr...
Deficient homozygosity of a variant maintained in a population suggests that the variant may be emb...
Standardized benchmarking approaches are required to assess the accuracy of variants called from seq...
The final product of our variant calling pipeline; obtained as described under: "Variant calling, fi...
Motivation: Whole-genome high-coverage sequencing has been widely used for personal and cancer genom...
<p>Presentation at Genome Informatics 2013:</p> <p> </p> <p>Translational research relies on accurat...
Whole Exome Sequencing (WES) is used for querying DNA variants using the protein coding parts of gen...
abstract: Analyzing human DNA sequence data allows researchers to identify variants associated with ...
Discovery of genome-wide variation has taken a huge leap forward with the introduction of next-gener...
Improvement of variant calling in next-generation sequence data requires a comprehensive, genome-wid...
<p>Variant calling data from whole-genome sequencing of the Jurkat cell line. The data set includes ...
Summary of the variants called across the four resequenced Norwich Terriers using Platypus within th...
<p>Results from variant calling in the three workflows MiSEQ Reporter 2.1.43 (GATK variant caller), ...
<div><p>A diversity of tools is available for identification of variants from genome sequence data. ...
PEMapper and PECaller are paired software programs that simplify mapping and variant calling for who...
Deficient homozygosity of a variant maintained in a population suggests that the variant may be embr...
Deficient homozygosity of a variant maintained in a population suggests that the variant may be emb...
Standardized benchmarking approaches are required to assess the accuracy of variants called from seq...