SNVer is a statistical tool for calling common and rare variants in analysis of pool or individual next-generation sequencing data. It reports one single overall p-value for evaluating the significance of a candidate locus being a variant, based on which multiplicity control can be obtained. Loci with any (low) coverage can be tested and depth of coverage will be quantitatively factored into final significance calculation. SNVer runs very fast, making it feasible for analysis of whole-exome sequencing data, or even whole-genome sequencing data.

Installers

Info: This package contains files in non-standard labels.

conda install

  • noarch  v0.5.3
To install this package with conda run one of the following:
conda install -c bioconda snver
conda install -c bioconda/label/cf201901 snver

Description

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