Topic

bioinformatics

Repositories (1500)

EDGE
EDGE LANL-Bioinformatics Perl

EDGE is a highly adaptable bioinformatics platform that allows laboratories to quickly analyze and interpret genomic sequence data.

79
hypeR
hypeR montilab R

An R Package for Geneset Enrichment Workflows

79
NeoDTI
NeoDTI FangpingWan Python

NeoDTI: Neural integration of neighbor information from a heterogeneous network for discovering new drug-target interactions

79
asap
asap oschwengers Groovy

A scalable bacterial genome assembly, annotation and analysis pipeline

79
cwl-svg
cwl-svg rabix TypeScript

A library for generating an interactive SVG visualization of CWL workflows

78
haslr
haslr vpc-ccg C++

A fast tool for hybrid genome assembly of long and short reads

78
BIGSdb
BIGSdb kjolley Perl

Bacterial Isolate Genome Sequence Database (BIGSdb): A platform for gene-by-gene bacterial population annotation and analysis.

78
harpy
harpy saeyslab Python

Single-cell spatial omics analysis that makes you happy!

78
EBImage
EBImage aoles R

:art: Image processing toolbox for R

77
pathogen-informatics-training
pathogen-informatics-training sanger-pathogens Jupyter Notebook
77
metage2metabo
metage2metabo AuReMe Jupyter Notebook

From annotated genomes to metabolic screening in large scale microbiotas

77
pyobo
pyobo biopragmatics Python

đź“› A Python package for using ontologies, terminologies, and biomedical nomenclatures

77
enrichment_analysis
enrichment_analysis epigen Python

A Snakemake workflow and MrBiomics module for performing genomic region set and gene set enrichment analyses using LOLA, GREAT, GSEApy, pycisTarget an...

77
top-pharma50
top-pharma50 servierhub Makefile

Top open source software from the top 50 pharmaceutical companies

77
AlterLab-Academic-Skills
AlterLab-Academic-Skills AlterLab-IEU Python

242 evaluated academic Claude/agent skills across 18 research domains — bioinformatics, cheminformatics, data science, databases, clinical, social sci...

77
mavis
mavis bcgsc Python

Merging, Annotation, Validation, and Illustration of Structural variants

76
GOSemSim
GOSemSim YuLab-SMU R

:golf: GO-terms Semantic Similarity Measures

76
panoptes
panoptes panoptes-organization CSS

Monitor computational workflows in real time

76
ClassifyCNV
ClassifyCNV Genotek Python

ClassifyCNV: a tool for clinical annotation of copy-number variants

76
aldy
aldy 0xTCG C

Allelic decomposition and exact genotyping of highly polymorphic and structurally variant genes

76
Contextualized
Contextualized AdaptInfer Python

An SKLearn-style toolbox for estimating and analyzing models, distributions, and functions with context-specific parameters.

76
nf-LO
nf-LO evotools Nextflow

A Nextflow workflow to generate lift over files for any pair of genomes

76
fast-collections
fast-collections Fast-Py Python

fast data structures and algorithms written in Rust, usable from Python.

76
oswitch
oswitch wurmlab Ruby

Provides access to complex Bioinformatics software (even BioLinux!) in just one command.

75
bfc
bfc lh3 TeX

High-performance error correction for Illumina resequencing data

75
bindash
bindash zhaoxiaofei C++

Fast and precise comparison of genomes and metagenomes (in the order of terabytes) on a typical personal laptop

75
NeuroSEED
NeuroSEED gcorso Python

Implementation of Neural Distance Embeddings for Biological Sequences (NeuroSEED) in PyTorch (NeurIPS 2021)

75
sequence_align
sequence_align kensho-technologies Python

Efficient implementations of Needleman-Wunsch and other sequence alignment algorithms written in Rust with Python bindings via PyO3.

75
TOmicsVis
TOmicsVis benben-miao R

Transcriptomics Visualization R package.

75
CompareM2
CompareM2 cmkobel Python

⚡🦠🧬📇 Rapid microbial genomes-to-report pipeline

75
depictio
depictio depictio Python

Bioinformatics web-platform visualisation dashboard creation

75
fermi
fermi lh3 C

A WGS de novo assembler based on the FMD-index for large genomes

74
sns
sns igordot Shell

Analysis pipelines for genomic sequencing data

74
CoGAPS
CoGAPS FertigLab C++

Bayesian MCMC matrix factorization algorithm

74
Toolkit
Toolkit proteinevolution Scala

The MPI Bioinformatics Toolkit

74
hic2cool
hic2cool 4dn-dcic Python

Lightweight converter between hic and cool contact matrices.

74
geneview
geneview ShujiaHuang Python

Genomics data visualization in Python by using matplotlib.

74
MEGADOCK
MEGADOCK akiyamalab C++

An ultra-high-performance protein-protein docking for heterogeneous supercomputers

74
dcHiC
dcHiC ay-lab R

dcHiC: Differential compartment analysis for Hi-C datasets

74
scMerge
scMerge SydneyBioX R

Statistical approach for removing unwanted variation from multiple single-cell datasets

74
make_lastz_chains
make_lastz_chains hillerlab Nextflow

Portable solution to generate genome alignment chains using lastz

74
salti
salti Sam-Sims Rust

A fast, feature rich multiple sequence alignment browser for the terminal.

74
tibanna
tibanna 4dn-dcic Python

Tibanna helps you run your genomic pipelines on Amazon cloud (AWS). It is used by the 4DN DCIC (4D Nucleome Data Coordination and Integration Center)...

73
Palimpsest
Palimpsest FunGeST R

An R package for studying mutational signatures and structural variant signatures along clonal evolution in cancer.

73
ontology-tutorial
ontology-tutorial bio-ontology-research-group Jupyter Notebook

Ontology Tutorial

73
Fastaq
Fastaq sanger-pathogens Python

Python3 scripts to manipulate FASTA and FASTQ files

73
uta
uta biocommons Python

Universal Transcript Archive: comprehensive genome-transcript alignments; multiple transcript sources, versions, and alignment methods; available as a...

73
zol
zol Kalan-Lab Python

zol (& fai): large-scale targeted detection and evolutionary investigation of gene clusters (i.e. BGCs, phages, etc.)

73
ggvolc
ggvolc loukesio R

Volcano plots for differential expression in R. Reads DESeq2, edgeR and limma output directly; highlight genes of interest and compose gene tables wit...

73
NEAT
NEAT ncsa Python

NEAT (NExt-generation Analysis Toolkit) simulates next-gen sequencing reads and can learn simulation parameters from real data.

73