Local-first genomics toolkit

Turn whole genome data into useful files, reports, and extracts.

WGS Extract CLI is a modern, scriptable command-line recreation of WGS Extract. It wraps common bioinformatics tools so you can inspect BAM/CRAM files, build consumer microarray files, call variants, extract Y/MT reads, manage references, and automate repeatable genome work.

A practical reference site, not just a splash page.

Use the pages below as a map for installing the tool, understanding WGS file types, and running common genome workflows safely.

Install

Install the standalone app or use Pixi directly

Use the standalone macOS/Linux installer, the native Windows installer, or the developer Pixi workflow when you want a normal source checkout.

Read the install guide
CLI reference

Command groups and recipes

Learn the major command families for info, BAM/CRAM, extraction, VCF calling, annotation, lineage, FASTQ QC, references, and fake data.

Open the CLI guide
Graphical interface

Want a GUI?

This package is CLI-only. Use gui-for-cli when you want a graphical interface for these workflows.

Workflows

Go from a goal to commands

Follow recipes for microarray simulation, Y-DNA and mtDNA extraction, variant calling, FASTQ to BAM, storage conversion, and testing.

Pick a workflow
WGS guide

Learn whole genome concepts

Get a friendly explanation of whole genome sequencing, coverage, references, variants, file types, read technologies, and interpretation limits.

Read the WGS guide
Reference

Glossary and safety notes

Look up common terms, file extensions, external tools, privacy considerations, and troubleshooting tips for long-running genome jobs.

Open the reference