From
http://www.broadinstitute.org/igv/viewing_vcf_files
VCF stands for Variant Call Format, and this file format is used by the
1000 Genomes project to encode SNPs and other structural genetic
variants. The format is further described on the
1000 Genomes project Web site. VCF calls are available at
EBI /
NCBI.
http://www.broadinstitute.org/software/igv/?q=download
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