Tools

VCF Normalize

Normalizes VCF variants: left-aligns indels, splits multiallelic sites. Required before variant annotation and downstream analysis.

Runnablealigned sequencing reads

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About this entry

Normalizes VCF variants: left-aligns indels, splits multiallelic sites. Required before variant annotation and downstream analysis.

CategoryTools

StatusRunnable

Inputaligned sequencing reads

Outputvariant calls

Use in DarwinOmics

How to use it

Use this tool to reproduce a concrete analysis step from supplied inputs, captured parameters, and versioned outputs, then compare the regenerated artifacts against the submitted result record.