Description

Annotate VCF files using pre-built SnpSift annMem databases. Enriches input VCF records by querying memory-optimized indexed dataframes for high-performance annotation.

Input

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Output

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Tools

snpsift Documentation

Genetic variant annotations and functional effect prediction toolbox

https://github.com/pcingola/SnpSiftdoi: 10.3389/fgene.2012.00035License: MIT
Authors