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, 17:28, 19 November 2009
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− | '''AnnoVcf''' is a [[SNP annotation]] tool for the next generation sequence data in the 1000 genome project. It takes a [[VCF]] SNP file as input and generates SNP annotation information into a VCF output | + | '''vcfCodingSnps''' is a [[SNP annotation]] tool that annotates coding variants in a [[VCF]] format input file. It takes a VCF as input and generates an annotated VCF file as output. |