Difference between revisions of "VcfCodingSnps"

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m (moved AnnoVcf to VcfCodingSnps: Better name)
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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
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'''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.

Revision as of 17:28, 19 November 2009

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.