Code mutations in your project or schematics were never easier than now.

Type safe and validated Server Actions in your Next.js (App Router) project.

Flu clade and mutation frequencies

🧟 Inject bugs and see if your tests catch them!

Converts JavaScript to TypeScript and TypeScript to better TypeScript. 🧫

Add WooCommerce support and functionality to your WPGraphQL server

Regexp based tool for mutating generic source code across numerous languages

Python GraphQL Client - PyGQLC

Build React forms based on GraphQL APIs.

EpiProfile 2.0: A Computational Platform for Processing Epi-Proteomics Mass Spectrometry Data

Matrix-like representations of mutation and CN data

A method to predict activating, deactivating and resistance mutations in kinases

nRex: Germline and somatic single-nucleotide, short indel and structural variant calling

🧬 Chromatogram File Utils, a package that integrates trace visualization, mutation calling and quality control for Sanger sequencing data.

curl for GraphQL with autocomplete, subscriptions and GraphiQL. Also a dead-simple universal javascript GraphQL client.

A tutorial on structural variant calling for short read sequencing data

Snakemake Pipeline for the Analyses of ChIP-seq data in Cancer samples

Ant Colony Optimization algorithm solving Google HashCode 2020 online elimination problem

Simple mutation-testing

The Cancer Genome Atlas (TCGA), a cancer genomics reference program, has molecularly characterized more than 20,000 primary cancer samples and paired normal samples covering 33 types of cancer. This joint effort between the NCI and the National Human Genome Research Institute began in 2006.