WebApps in pure Python. No JavaScript, HTML and CSS needed

SUPPA: Fast quantification of splicing and differential splicing

tools for adding mutations to existing .bam files, used for testing mutation callers

HUMAnN is the next generation of HUMAnN 1.0 (HMP Unified Metabolic Analysis Network).

Command-line tool for the visualization of splicing events across multiple samples

Deep Learning based cell composition analysis with Scaden.

A Variant Call Format reader for Python.

Meta-Omics Software for Community Analysis

Tool for computation of the minimal coverage depth for given variant allele frequency and probability of sequencing error.

Oncogenicity Variant Interpreter for somatic variants