vatools

A tool for annotating VCF files with expression and readcount data


Keywords
cancer, sequencing, variant, variants, gene, expression, readcounts, VAF, allele, frequency, FPKM, TPM, transcript, VCF
License
MIT
Install
pip install vatools==5.1.1

Documentation

VCF Annotation Tools (VAtools)

VCF Annotation Tools is a python package that includes several tools to annotate VCF files with data from other tools.

vcf-readcount-annotator

A tool that will add the data from bam-readcount files to the VCF sample column.

vcf-expression-annotator

A tool that will add the data from several expression tools’ output files to the VCF INFO column. Supported tools are StringTie, Kallisto, and Cufflinks. There also is a custom option to annotate with data from any tab-delimited file.

vcf-info-annotator

A tool that will add data from a tab-delimited file to any user-specified field in the VCF INFO column.

vcf-genotype-annotator

A tool to add a new sample to an existing VCF file.

vep-annotation-reporter

A tool to create a tab-delimited (TSV) file of variants in a VCF and their VEP annotations.

ref-transcript-mismatch-reporter

A tool to identify variants in a VCF where the reference genome used to align and call variants doesn't match the Ensembl reference transcript used by VEP for variant consequence annotations.

transform-split-values

A tool that extracts and manipulates values from existing sample fields and outputs the results to a TSV file.

Documentation

Please see vatools.org for the full documentation.

Install

pip install vatools