Command-line tools to expedite analysis of Variant Call Format (VCF) files.


Keywords
VCF, bioinformatic, exome-seq, DNA-seq, variant-call-format
License
Apache-2.0
Install
pip install jacquard==1.1.5

Documentation

Jacquard

Suite of command-line tools to expedite analysis of exome variant data from multiple patients and multiple variant callers.

Build Status Coverage Status License Latest PyPI version

The official repository is at:

https://github.com/umich-brcf-bioinf/Jacquard

Usage

$ jacquard <subcommand> [options] [arguments]

Subcommands

translate: Creates new VCFs, adding a controlled vocabulary of new FORMAT tags.
merge: Integrates a directory of VCFs into a single VCF.
summarize: Adds new INFO fields and FORMAT tags that combine variant data from the merged VCF.
expand: Explodes a VCF file into a tab-delimited file.

For help on a specific subcommand:

$ jacquard <subcommand> --help

See ReadTheDocs for full documentation.


Email bfx-jacquard@umich.edu for support and questions.

UM BRCF Bioinformatics Core