Open-source music player that turns your local library and connected sources into personalised listening journeys using Flow sequencing, taste memory, rediscovery, and optional LLM control.
Data intensive science for everyone.
An ultra-fast all-in-one FASTQ preprocessor (QC/adapters/trimming/filtering/splitting/merging...)
Tools (written in C using htslib) for manipulating next-generation sequencing data
RNA sequencing analysis pipeline using STAR, RSEM, HISAT2 or Salmon with gene/isoform counts and extensive quality control.
C library for high-throughput sequencing data formats
State-of-the-art bio cell models for inference and training. Minimal, readable, and produciton-ready.
Official code repository for GATK versions 4 and up
SPAdes Genome Assembler
Community-driven, simple, yet powerful framework for fast, cost-effective distributed Compute over Data.
Tools to process and analyze deep sequencing data.
Structural variation caller using third generation sequencing
A quality control analysis tool for high throughput sequencing data
Copy number variant detection from targeted DNA sequencing
Analysis pipeline to detect germline or somatic variants (pre-processing, variant calling and annotation) from WGS / targeted sequencing
Plotting scripts for long read sequencing data
Java utilities for Bioinformatics
RhythmFlow Pro 2026: Advanced Rhythmic Sequencing for Musicians
Choreograph SwiftUI animations into ordered sequences of steps.
DeepVariant is an analysis pipeline that uses a deep neural network to call genetic variants from next-generation DNA sequencing data.
Genomic sequence storage, indexing and alignment inside PostgreSQL: https://bioseqdb.com/