1000_genomes:analysis:variant_call_format [1000 Genomes]
This page is to support discussion of the draft spec for the Variant Call Format (VCF), in which the 1000 Genomes SNP and short indel calls will be released. There is currently a proposal on the table for a new version of VCF VCF4.0 (drafted May 12th, 2010). The aim of this update is to improve the various data types and missing values used in the VCF file and to derive a consensus for placing sho
GATK
Genome Analysis Toolkit Variant Discovery in High-Throughput Sequencing Data Need Help? Search our documentation Community Forum Hi, How can we help? Developed in the Data Sciences Platform at the Broad Institute, the toolkit offers a wide variety of tools with a primary focus on variant discovery and genotyping. Its powerful processing engine and high-performance computing features make it capabl
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