classify.variant

<p>Classify a variant as SNV, MNV, or indel based on the reference and alternative alleles</p>

Multi-caller variant analysis pipeline for targeted analysis sequencing (TAS) data. Features a modular, automated workflow that can start with raw reads and produces a user-friendly PDF summary and a spreadsheet containing consensus variant information.

Adam Mills

varitas

Variant Calling in Targeted Analysis Sequencing Data

classify.variant: classify.variant

Description

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