Python library to facilitate genome assembly, annotation, and comparative genomics
Pysam is a Python package for reading, manipulating, and writing genomics data such as SAM/BAM/CRAM and VCF/BCF files. It's a lightweight wrapper of t...
🔬🦞 A self-evolving AI research colleague for scientists. 285 skills, zero hallucination, persistent memory.
A curated list of Cheminformatics libraries and software.
The next version of bwa-mem
Specification for the Workflow Description Language (WDL).
Plant phenotyping with image analysis
Precision Medicine Knowledge Graph (PrimeKG)
Bioinformatics containers
Hifiasm: a haplotype-resolved assembler for accurate Hifi reads
A fast and sensitive gapped read aligner
Python package for graph neural networks in chemistry and biology
Python and C++ code for reading and writing genomics data.
In-memory nucleotide sequence k-mer counting, filtering, graph traversal and more
Annotated data.
Tools to process and analyze deep sequencing data.
A Python implementation of the DESeq2 pipeline for bulk RNA-seq DEA.
Versatile open-source tool for microbiome analysis
Working with molecular structures in pandas DataFrames
A Go package for engineering organisms.
Ultra-fast and memory-efficient (meta-)genome assembler
Protein-Ligand Interaction Profiler - Analyze and visualize non-covalent protein-ligand interactions in PDB files according to 📝 Schake, Bolz, et al....
A high-performance, Pythonic language for bioinformatics
:eye: Python library to plot DNA sequence features (e.g. from Genbank files)
Rapid & standardized annotation of bacterial genomes, MAGs & plasmids
Interactive network visualization in Python and Dash, powered by Cytoscape.js
Structural variation caller using third generation sequencing
High-school research portfolio: 2 peer-reviewed publications (IEEE, IJHSR) + 3 active projects spanning quantum-inspired ML, computational biology, bi...
ScienceClaw is a personal research assistant built with LangChain DeepAgents and AIO Sandbox infrastructure, adopting a completely new architecture be...
Cell type annotation for single-cell RNA-seq using multi-LLM consensus
Gene cluster comparison figure generator
A scikit-learn compatible library for graph kernels
BWK awk modified for biological data
BioMCP: Biomedical Model Context Protocol
:book::microscope::coffee: BioJava is an open-source project dedicated to providing a Java library for processing biological data.
Remote protein homology detection suite.
GTDB-Tk: a toolkit for assigning objective taxonomic classifications to bacterial and archaeal genomes.
Tools for working with SAM/BAM data
Lightweight, super fast C/C++ (& Python) library for sequence alignment using edit (Levenshtein) distance.
The Chemistry Development Kit
Analysis pipeline to detect germline or somatic variants (pre-processing, variant calling and annotation) from WGS / targeted sequencing
Signal-level algorithms for MinION data
Yet another redundant workflow engine
:scissors: :zap: Rapid haploid variant calling and core genome alignment
Biostar Q&A
COBRApy is a package for constraint-based modeling of metabolic networks.
Cutadapt removes adapter sequences from sequencing reads
Open-source bioinformatics components for Dash
Accurate sample inference from amplicon data with single nucleotide resolution
Quickly search, compare, and analyze genomic and metagenomic data sets.