Scripts for analyzing tandem repeat sequences in long-read data

A curated list of awesome genomics and bioinformatics agentic skills, MCPs and benchmarks for Claude Code, Copilot, Codex, Cursor, Gemini CLI, etc

Nextflow pipeline to analyze ONT-UMI-Sequencing data

Python drop-in replacement for PyHPO using Rust

SDrecall is designed for sensitive variant detection in segmental duplications

macOS transliteration input method for Russian, Hebrew, Ukrainian and Belarusian

A collection of my favorite custom Claude Code resources to make life easier.

A tool for estimating the copy number of large tandem repeats

a python package for finding tandem repeats from genomic sequences

Python interactive dashboards for learning data science

Reads simulator

With Django Hijack, admins can log in and work on behalf of other users without having to know their credentials.

Elasticsearch cluster on top of Kubernetes made easy.

Random Forest classifier classifies Expansion Hunter expansions as true or false

Short Tandem Repeat disease loci resource

⬆️ GitHub Actions uptime monitor & status page by @AnandChowdhary

A simple macOS application that will prevent iTunes or Apple Music from launching.

The complete sequence of a human genome

All Algorithms implemented in Rust

Add deep anchor links to your docs.

Copy number estimation and variant calling for duplicated genes using WGS.

A tool to find sequencing data and metadata from public databases.

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Glances an Eye on your system. A top/htop alternative for GNU/Linux, BSD, macOS and Windows operating systems.

CLI for interacting with Cromwell servers