GalaxyData intensive science for everyone.
Stars: ✭ 812 (+703.96%)
catchA package for designing compact and comprehensive capture probe sets.
Stars: ✭ 55 (-45.54%)
UgeneUGENE is free open-source cross-platform bioinformatics software
Stars: ✭ 112 (+10.89%)
GatkOfficial code repository for GATK versions 4 and up
Stars: ✭ 1,002 (+892.08%)
DeepvariantDeepVariant is an analysis pipeline that uses a deep neural network to call genetic variants from next-generation DNA sequencing data.
Stars: ✭ 2,404 (+2280.2%)
SnsAnalysis pipelines for sequencing data
Stars: ✭ 43 (-57.43%)
HtsjdkA Java API for high-throughput sequencing data (HTS) formats.
Stars: ✭ 220 (+117.82%)
Rnaseq WorkflowA repository for setting up a RNAseq workflow
Stars: ✭ 170 (+68.32%)
Tiledb VcfEfficient variant-call data storage and retrieval library using the TileDB storage library.
Stars: ✭ 26 (-74.26%)
gff3toemblConverts Prokka GFF3 files to EMBL files for uploading annotated assemblies to EBI
Stars: ✭ 27 (-73.27%)
ArvadosAn open source platform for managing and analyzing biomedical big data
Stars: ✭ 274 (+171.29%)
PyfaidxEfficient pythonic random access to fasta subsequences
Stars: ✭ 307 (+203.96%)
RoaryRapid large-scale prokaryote pan genome analysis
Stars: ✭ 176 (+74.26%)
SarekDetect germline or somatic variants from normal or tumour/normal whole-genome or targeted sequencing
Stars: ✭ 124 (+22.77%)
NucleusPython and C++ code for reading and writing genomics data.
Stars: ✭ 657 (+550.5%)
NglessNGLess: NGS with less work
Stars: ✭ 115 (+13.86%)
ArtemisArtemis is a free genome viewer and annotation tool that allows visualization of sequence features and the results of analyses within the context of the sequence, and its six-frame translation
Stars: ✭ 135 (+33.66%)
CirclatorA tool to circularize genome assemblies
Stars: ✭ 121 (+19.8%)
HgvsPython library to parse, format, validate, normalize, and map sequence variants. `pip install hgvs`
Stars: ✭ 138 (+36.63%)
Helmsmanhighly-efficient & lightweight mutation signature matrix aggregation
Stars: ✭ 19 (-81.19%)
Cyvcf2cython + htslib == fast VCF and BCF processing
Stars: ✭ 243 (+140.59%)
BiopythonOfficial git repository for Biopython (originally converted from CVS)
Stars: ✭ 2,936 (+2806.93%)
AribaAntimicrobial Resistance Identification By Assembly
Stars: ✭ 96 (-4.95%)
JvarkitJava utilities for Bioinformatics
Stars: ✭ 313 (+209.9%)
dna-traitsA fast 23andMe genome text file parser, now superseded by arv
Stars: ✭ 64 (-36.63%)
SequenceserverIntuitive local web frontend for the BLAST bioinformatics tool
Stars: ✭ 198 (+96.04%)
HailScalable genomic data analysis.
Stars: ✭ 706 (+599.01%)
Hap.pyHaplotype VCF comparison tools
Stars: ✭ 249 (+146.53%)
adaptA package for designing activity-informed nucleic acid diagnostics for viruses.
Stars: ✭ 16 (-84.16%)
saffrontreeSaffronTree: Reference free rapid phylogenetic tree construction from raw read data
Stars: ✭ 17 (-83.17%)
Bio.jl[DEPRECATED] Bioinformatics and Computational Biology Infrastructure for Julia
Stars: ✭ 257 (+154.46%)
awesome-geneticsA curated list of awesome bioinformatics software.
Stars: ✭ 60 (-40.59%)
GubbinsRapid phylogenetic analysis of large samples of recombinant bacterial whole genome sequences using Gubbins
Stars: ✭ 67 (-33.66%)
TruvariStructural variant toolkit for VCFs
Stars: ✭ 85 (-15.84%)
Fastq.bioAn interactive web tool for quality control of DNA sequencing data
Stars: ✭ 76 (-24.75%)
PygenoPersonalized Genomics and Proteomics. Main diet: Ensembl, side dishes: SNPs
Stars: ✭ 261 (+158.42%)
plasmidtronAssembling the cause of phenotypes and genotypes from NGS data
Stars: ✭ 27 (-73.27%)
Vcfannoannotate a VCF with other VCFs/BEDs/tabixed files
Stars: ✭ 259 (+156.44%)
SvtyperBayesian genotyper for structural variants
Stars: ✭ 79 (-21.78%)
MegahitUltra-fast and memory-efficient (meta-)genome assembler
Stars: ✭ 343 (+239.6%)
NanopolishSignal-level algorithms for MinION data
Stars: ✭ 367 (+263.37%)
Gwa tutorialA comprehensive tutorial about GWAS and PRS
Stars: ✭ 303 (+200%)
PlantcvPlant image analysis using OpenCV
Stars: ✭ 352 (+248.51%)
BioBioinformatics library for .NET
Stars: ✭ 90 (-10.89%)
JcviPython library to facilitate genome assembly, annotation, and comparative genomics
Stars: ✭ 404 (+300%)
JbrowseA modern genome browser built with JavaScript and HTML5.
Stars: ✭ 393 (+289.11%)
Bwa Mem2The next version of bwa-mem
Stars: ✭ 408 (+303.96%)
SmudgeplotInference of ploidy and heterozygosity structure using whole genome sequencing data
Stars: ✭ 98 (-2.97%)
Bowtie2A fast and sensitive gapped read aligner
Stars: ✭ 365 (+261.39%)
Biojava📖🔬☕️ BioJava is an open-source project dedicated to providing a Java library for processing biological data.
Stars: ✭ 434 (+329.7%)
HtslibC library for high-throughput sequencing data formats
Stars: ✭ 529 (+423.76%)
DeeptoolsTools to process and analyze deep sequencing data.
Stars: ✭ 448 (+343.56%)
KhmerIn-memory nucleotide sequence k-mer counting, filtering, graph traversal and more
Stars: ✭ 640 (+533.66%)
CromwellScientific workflow engine designed for simplicity & scalability. Trivially transition between one off use cases to massive scale production environments
Stars: ✭ 655 (+548.51%)
Vgtools for working with genome variation graphs
Stars: ✭ 710 (+602.97%)