A lightweight and powerful Julia package for computational pipelines and workflows.
AI and Omics Research Internship 2025
A Snakemake workflow and MrBiomics module to split, filter, normalize, integrate and select highly variable features of count matrices resulting from...
RabbitTClust: enabling fast clustering analysis of millions bacteria genomes with MinHash sketches
Fast, Accurate and Memory-Efficient Principal Component Analysis All in One For Large-scale Dataset
Read mapping pipeline for detection and measurement of virus pathogens from metagenomic or clinical data
Repository to propose and discuss lineages
충남대학교 김준 연구실 튜토리얼
Activity-Oriented Enzyme Sequence Design by Steered Inverse Protein Folding
An agent that takes a dead research repo and turns it into a callable pipeline component.
Natural language processing of Gene Expression Omnibus data
BioContainers specifications
🧬 Toolkit for generating various numerical features of protein sequences
Deep (Transfer) Learning for Peptide Retention Time Prediction
Phigaro is a scalable command-line tool for predicting phages and prophages
Multiple-particle tracking designed to (1) track dense particle fields, (2) close gaps in particle trajectories resulting from detection failure, and...
A versatile compressor of third generation sequencing reads.
This repository contains Docker files for the images maintained by the Phenotypic Evolution Group at the Institute for Molecular and Cell Biology / In...
Scalable SQLite database for fast querying of gnomAD variant annotations (allele frequency, depth, population metrics). Supports gnomAD v2-v4, WGS and...
Ribo-seq TIS Hunter, predicting translation initiation sites and ORFs using riboseq data
StrainDesign is a python package for the computational design of metabolic networks and based on COBRApy
Minimizer-based assembly scaffolding and mapping using long reads
A tool for the recovery of unassembled telomeres from soft-clipped read alignments.
Meet FIORA! An in silico fragmentation algorithm designed to predict tandem mass spectra (MS/MS) with high accuracy. Using graph neural networks, FIOR...
Information-Theoretic Measures for Revealing Variable Interactions
A manifesto for AI-assisted modernisation of bioinformatics software.
Collection of commonly used RDP Tools for easy building
Cloud-based single-cell copy-number variation analysis tool
Pipeline for structural variation detection in cohorts
an implementation of NSGA-II in java
non-redundant, compressed, journalled, file-based storage for biological sequences
A python package and a set of shell commands to handle GTF files
Precision psychophysiology made easy
Fast and flexible semi-supervised learning for peptide detection in Python
Close assembly gaps using long-reads at high accuracy.
:comet: Ultrafast DNA methylation heterogeneity calculation from bisulfite alignments (Lee et al., PLOS Computational Biology. 2023)
Claude-Code for Bioinformatics
Tool suite for HGVS variant descriptions
BRIG is a cross-platform (Windows/Mac/Linux) application that displays circular comparison images of multiple genomes using BLAST.
A fragment-based molecular assembly toolkit
Parse Illumina sample sheets with Python
Exact Tandem Repeat Finder (not a TRF replacement)
A simple command-line tool to download data from Joint Genome Institute databases
A reimplementation of the WaveFront Alignment algorithm at low memory
Identifying tumor cells at the single-cell level using machine learning
A Python package for obtaining, parsing and exploring biological taxonomies (GTDB, NCBI, Silva, Greengenes, OTT)
ChatCell: Facilitating Single-Cell Analysis with Natural Language
Remove human reads from a sequencing run
Transmembrane proteins predicted through Language Model embeddings
CellNavi is a deep learning framework designed to predict genes driving cellular transitions.