Turn any AI agent into an AI Scientist. The #1 Agent Skills library for science, used by 250,000+ scientists worldwide. 177 ready-to-use validated skills plus 100+ scientific databases covering biology, chemistry, medicine, and drug discovery. Compatible with Cursor, Claude Code, Codex, Pi, Antigravity, and the open Agent Skills standard.
Repository Index
47,133 repositories indexed
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Official git repository for Biopython (originally converted from CVS)
Deep probabilistic analysis of single-cell and spatial omics data
🦖 ClawBio - The first bioinformatics-native AI agent skill library. Local-first. Reproducible. Open. Free.
Cloud-native genomic dataframes and batch computing
ADAM is a genomics analysis platform with specialized file formats built using Apache Avro, Apache Spark, and Apache Parquet. Apache 2 licensed.
Foundation Models for Genomics & Transcriptomics
Official implementation for HyenaDNA, a long-range genomic foundation model built with Hyena
C++ library and cmdline tools for parsing and manipulating VCF files with python and zig bindings
Fast, sensitive and accurate integration of single-cell data with Harmony
Spatial Single Cell Analysis in Python
Reference mapping for single-cell genomics
Genomic Pretrained Network - GPN, GPN-MSA, PhyloGPN, GPN-Star
Fusing Histology and Genomics via Deep Learning - IEEE TMI
Pan-Cancer Integrative Histology-Genomic Analysis via Multimodal Deep Learning - Cancer Cell
Haplotype-aware CNV analysis from single-cell RNA-seq, ATAC-seq, and multiome
Genomic sequence storage, indexing and alignment inside PostgreSQL: https://bioseqdb.com/
Code for "Predicting Cellular Responses to Novel Drug Perturbations at a Single-Cell Resolution", NeurIPS 2022.
CASSIA: A Multi-Agent LLM-Based Single-Cell Cell Type Annotation Framework
Peax is a tool for interactive visual pattern search and exploration in epigenomic data based on unsupervised representation learning with autoencoders
Autonomous multi-agent framework to optimize scientific software
MCP server for spatial transcriptomics analysis through natural language interfaces.
Multigrate: multiomic data integration for single-cell genomics
Vendor-agnostic, FHIR-Genomics-aligned API contract for cross-vendor NGS interpretation. JSON Schema + TypeScript + Python pydantic.