
Biopython
The foundational open-source library for biological computation and bioinformatics in Python.

The foundational open-source library for biological computation and bioinformatics in Python.
Seurat is an R package designed for single-cell RNA-seq data analysis, exploration, and integration of diverse single-cell data types.

Accelerating biological discovery through open-source software and AI-driven research workflows.

The premier open-source genomic workflow system for reproducible scientific research and advanced omics analysis.
The AI-Ready Data Platform for Biomedical Data

Advanced gene function prediction and association network integration for precision genomics.
AI-driven genomic data analysis and variant interpretation platform.

STRING is a database of known and predicted protein-protein interactions.

The gold-standard database of experimentally validated metabolic pathways and biochemical reactions.
Galaxy is a web-based platform for data intensive biomedical research.

A versatile pairwise aligner for genomic and spliced nucleotide sequences.

The foundational open-access repository for curated protein and genetic interaction datasets.

The global backbone for biomedical data, genomic intelligence, and clinical research informatics.

Gamified Protein Folding: Harnessing human intuition to solve complex biochemical puzzles for drug discovery.

A fast spliced aligner for RNA-seq data.

The open-source ecosystem for data-intensive science, workflow automation, and reproducible research.

A software package for mapping DNA sequences against a large reference genome.
Monocle is a toolkit for analyzing single-cell RNA-seq data, enabling researchers to build trajectories, classify cells, and find differentially expressed genes.

Petascale parallel molecular dynamics for high-fidelity biomolecular simulations.

The Industry Standard for Protein Comparative Modeling and Structural Bio-Refinement.
ModelSEED is a computational platform for genome-scale metabolic model reconstruction and analysis.

The gold standard for biological pathway mapping and genomic functional annotation.

The industry-standard engine for high-throughput genomic variant discovery and clinical-grade sequencing analysis.

Scalable toolkit for analyzing single-cell gene expression data in Python.

A workflow for pre-processing single-cell RNA-seq data, enabling cell x gene matrix generation and analysis.

Empowering local laboratories with automated, IVD-cleared genomic profiling for precision oncology.
The Human Protein Atlas is an open-access resource that maps all human proteins in cells, tissues, and organs.

Systematic drug target identification and prioritization through large-scale genomic and clinical data integration.

The all-in-one bioinformatics platform for high-performance NGS data analysis and functional interpretation.
WikiPathways is an open science platform for biological pathways contributed, updated, and used by the research community.

The premier multi-omics discovery index for cross-repository data orchestration and meta-analysis.

The gold standard for high-throughput genomic data analysis and reproducible bioinformatics.
EMBL-EBI provides freely available data resources and bioinformatics services to the scientific community, supporting research and innovation in molecular biology and related fields.

The industry-standard interactive visualization tool for integrated exploration of large-scale genomic datasets.

High-performance computational biology and bioinformatics infrastructure for the Julia language.
Spliced Transcripts Alignment to a Reference (STAR) is an ultrafast RNA-seq aligner.
Reactome is a free, open-source, curated and peer-reviewed pathway database for visualizing, interpreting and analyzing pathway knowledge.