SnsAnalysis pipelines for sequencing data
Stars: ✭ 43 (-98.54%)
GalaxyData intensive science for everyone.
Stars: ✭ 812 (-72.34%)
Bio.jl[DEPRECATED] Bioinformatics and Computational Biology Infrastructure for Julia
Stars: ✭ 257 (-91.25%)
NucleusPython and C++ code for reading and writing genomics data.
Stars: ✭ 657 (-77.62%)
lightdockProtein-protein, protein-peptide and protein-DNA docking framework based on the GSO algorithm
Stars: ✭ 110 (-96.25%)
GenomicsA collection of scripts and notes related to genomics and bioinformatics
Stars: ✭ 101 (-96.56%)
orfipyFast and flexible ORF finder
Stars: ✭ 27 (-99.08%)
unimapA EXPERIMENTAL fork of minimap2 optimized for assembly-to-reference alignment
Stars: ✭ 76 (-97.41%)
BuddySuiteBioinformatics toolkits for manipulating sequence, alignment, and phylogenetic tree files
Stars: ✭ 106 (-96.39%)
awesome-geneticsA curated list of awesome bioinformatics software.
Stars: ✭ 60 (-97.96%)
GatkOfficial code repository for GATK versions 4 and up
Stars: ✭ 1,002 (-65.87%)
DeepvariantDeepVariant is an analysis pipeline that uses a deep neural network to call genetic variants from next-generation DNA sequencing data.
Stars: ✭ 2,404 (-18.12%)
catchA package for designing compact and comprehensive capture probe sets.
Stars: ✭ 55 (-98.13%)
deepblastNeural Networks for Protein Sequence Alignment
Stars: ✭ 29 (-99.01%)
dna-traitsA fast 23andMe genome text file parser, now superseded by arv
Stars: ✭ 64 (-97.82%)
PyfaidxEfficient pythonic random access to fasta subsequences
Stars: ✭ 307 (-89.54%)
Vgtools for working with genome variation graphs
Stars: ✭ 710 (-75.82%)
Bedops🔬 BEDOPS: high-performance genomic feature operations
Stars: ✭ 215 (-92.68%)
RibbonA genome browser that shows long reads and complex variants better
Stars: ✭ 184 (-93.73%)
Minimap2A versatile pairwise aligner for genomic and spliced nucleotide sequences
Stars: ✭ 912 (-68.94%)
BwaBurrow-Wheeler Aligner for short-read alignment (see minimap2 for long-read alignment)
Stars: ✭ 970 (-66.96%)
Janggu Deep learning infrastructure for bioinformatics
Stars: ✭ 174 (-94.07%)
Deep RulesTen Quick Tips for Deep Learning in Biology
Stars: ✭ 179 (-93.9%)
BgtFlexible genotype query among 30,000+ samples whole-genome
Stars: ✭ 72 (-97.55%)
Fastq.bioAn interactive web tool for quality control of DNA sequencing data
Stars: ✭ 76 (-97.41%)
HailScalable genomic data analysis.
Stars: ✭ 706 (-75.95%)
Cyvcf2cython + htslib == fast VCF and BCF processing
Stars: ✭ 243 (-91.72%)
GenometoolsGenomeTools genome analysis system.
Stars: ✭ 186 (-93.66%)
Goleftgoleft is a collection of bioinformatics tools distributed under MIT license in a single static binary
Stars: ✭ 175 (-94.04%)
SibeliazA fast whole-genome aligner based on de Bruijn graphs
Stars: ✭ 76 (-97.41%)
BowtieAn ultrafast memory-efficient short read aligner
Stars: ✭ 221 (-92.47%)
MinigraphProof-of-concept seq-to-graph mapper and graph generator
Stars: ✭ 206 (-92.98%)
Tiledb VcfEfficient variant-call data storage and retrieval library using the TileDB storage library.
Stars: ✭ 26 (-99.11%)
KhmerIn-memory nucleotide sequence k-mer counting, filtering, graph traversal and more
Stars: ✭ 640 (-78.2%)
GubbinsRapid phylogenetic analysis of large samples of recombinant bacterial whole genome sequences using Gubbins
Stars: ✭ 67 (-97.72%)
Dna NnModel and predict short DNA sequence features with neural networks
Stars: ✭ 59 (-97.99%)
WgsimReads simulator
Stars: ✭ 178 (-93.94%)
DramDistilled and Refined Annotation of Metabolism: A tool for the annotation and curation of function for microbial and viral genomes
Stars: ✭ 47 (-98.4%)
RoaryRapid large-scale prokaryote pan genome analysis
Stars: ✭ 176 (-94.01%)
SvtyperBayesian genotyper for structural variants
Stars: ✭ 79 (-97.31%)
AribaAntimicrobial Resistance Identification By Assembly
Stars: ✭ 96 (-96.73%)
SmudgeplotInference of ploidy and heterozygosity structure using whole genome sequencing data
Stars: ✭ 98 (-96.66%)
BioBioinformatics library for .NET
Stars: ✭ 90 (-96.93%)
CgrangesA C/C++ library for fast interval overlap queries (with a "bedtools coverage" example)
Stars: ✭ 111 (-96.22%)
UgeneUGENE is free open-source cross-platform bioinformatics software
Stars: ✭ 112 (-96.19%)
HicexplorerHiCExplorer is a powerful and easy to use set of tools to process, normalize and visualize Hi-C data.
Stars: ✭ 116 (-96.05%)
NglessNGLess: NGS with less work
Stars: ✭ 115 (-96.08%)
SequenceserverIntuitive local web frontend for the BLAST bioinformatics tool
Stars: ✭ 198 (-93.26%)
HtsjdkA Java API for high-throughput sequencing data (HTS) formats.
Stars: ✭ 220 (-92.51%)
CoolerA cool place to store your Hi-C
Stars: ✭ 112 (-96.19%)
CirclatorA tool to circularize genome assemblies
Stars: ✭ 121 (-95.88%)
IntermineA powerful open source data warehouse system
Stars: ✭ 195 (-93.36%)
Hts Nimnim wrapper for htslib for parsing genomics data files
Stars: ✭ 132 (-95.5%)
Somalierfast sample-swap and relatedness checks on BAMs/CRAMs/VCFs/GVCFs... "like damn that is one smart wine guy"
Stars: ✭ 128 (-95.64%)
OctopusBayesian haplotype-based mutation calling
Stars: ✭ 131 (-95.54%)