GenomicDataCommonsProvide R access to the NCI Genomic Data Commons portal.
Stars: ✭ 64 (+88.24%)
Somalierfast sample-swap and relatedness checks on BAMs/CRAMs/VCFs/GVCFs... "like damn that is one smart wine guy"
Stars: ✭ 128 (+276.47%)
faster lmm dA faster lmm for GWAS. Supports GPU backend.
Stars: ✭ 12 (-64.71%)
OctopusBayesian haplotype-based mutation calling
Stars: ✭ 131 (+285.29%)
Fastq.bioAn interactive web tool for quality control of DNA sequencing data
Stars: ✭ 76 (+123.53%)
GenomicsqliteGenomics Extension for SQLite
Stars: ✭ 90 (+164.71%)
NglessNGLess: NGS with less work
Stars: ✭ 115 (+238.24%)
HicexplorerHiCExplorer is a powerful and easy to use set of tools to process, normalize and visualize Hi-C data.
Stars: ✭ 116 (+241.18%)
DeepvariantDeepVariant is an analysis pipeline that uses a deep neural network to call genetic variants from next-generation DNA sequencing data.
Stars: ✭ 2,404 (+6970.59%)
Janggu Deep learning infrastructure for bioinformatics
Stars: ✭ 174 (+411.76%)
SequenceserverIntuitive local web frontend for the BLAST bioinformatics tool
Stars: ✭ 198 (+482.35%)
GubbinsRapid phylogenetic analysis of large samples of recombinant bacterial whole genome sequences using Gubbins
Stars: ✭ 67 (+97.06%)
BgtFlexible genotype query among 30,000+ samples whole-genome
Stars: ✭ 72 (+111.76%)
Scaff10XPipeline for scaffolding and breaking a genome assembly using 10x genomics linked-reads
Stars: ✭ 21 (-38.24%)
SibeliazA fast whole-genome aligner based on de Bruijn graphs
Stars: ✭ 76 (+123.53%)
jgi-queryA simple command-line tool to download data from Joint Genome Institute databases
Stars: ✭ 38 (+11.76%)
CgrangesA C/C++ library for fast interval overlap queries (with a "bedtools coverage" example)
Stars: ✭ 111 (+226.47%)
SarekDetect germline or somatic variants from normal or tumour/normal whole-genome or targeted sequencing
Stars: ✭ 124 (+264.71%)
RoaryRapid large-scale prokaryote pan genome analysis
Stars: ✭ 176 (+417.65%)
WgsimReads simulator
Stars: ✭ 178 (+423.53%)
dysgudysgu-SV is a collection of tools for calling structural variants using short or long reads
Stars: ✭ 47 (+38.24%)
RibbonA genome browser that shows long reads and complex variants better
Stars: ✭ 184 (+441.18%)
Cyvcf2cython + htslib == fast VCF and BCF processing
Stars: ✭ 243 (+614.71%)
DashAnalytical Web Apps for Python, R, Julia, and Jupyter. No JavaScript Required.
Stars: ✭ 15,592 (+45758.82%)
CanvasxpressJavaScript VisualizationTools
Stars: ✭ 247 (+626.47%)
unimapA EXPERIMENTAL fork of minimap2 optimized for assembly-to-reference alignment
Stars: ✭ 76 (+123.53%)
Dna NnModel and predict short DNA sequence features with neural networks
Stars: ✭ 59 (+73.53%)
wgs2ncbiToolkit for preparing genomes for submission to NCBI
Stars: ✭ 25 (-26.47%)
DramDistilled and Refined Annotation of Metabolism: A tool for the annotation and curation of function for microbial and viral genomes
Stars: ✭ 47 (+38.24%)
Awesome 10x GenomicsList of tools and resources related to the 10x Genomics GEMCode/Chromium system
Stars: ✭ 82 (+141.18%)
SvtyperBayesian genotyper for structural variants
Stars: ✭ 79 (+132.35%)
BioBioinformatics library for .NET
Stars: ✭ 90 (+164.71%)
SnsAnalysis pipelines for sequencing data
Stars: ✭ 43 (+26.47%)
GenomicsA collection of scripts and notes related to genomics and bioinformatics
Stars: ✭ 101 (+197.06%)
SmudgeplotInference of ploidy and heterozygosity structure using whole genome sequencing data
Stars: ✭ 98 (+188.24%)
CoolerA cool place to store your Hi-C
Stars: ✭ 112 (+229.41%)
AribaAntimicrobial Resistance Identification By Assembly
Stars: ✭ 96 (+182.35%)
Kmer CntCode examples of fast and simple k-mer counters for tutorial purposes
Stars: ✭ 124 (+264.71%)
CirclatorA tool to circularize genome assemblies
Stars: ✭ 121 (+255.88%)
Hts Nimnim wrapper for htslib for parsing genomics data files
Stars: ✭ 132 (+288.24%)
LigerLightweight Iterative Gene set Enrichment in R
Stars: ✭ 44 (+29.41%)
Goleftgoleft is a collection of bioinformatics tools distributed under MIT license in a single static binary
Stars: ✭ 175 (+414.71%)
Deep RulesTen Quick Tips for Deep Learning in Biology
Stars: ✭ 179 (+426.47%)
HgvsPython library to parse, format, validate, normalize, and map sequence variants. `pip install hgvs`
Stars: ✭ 138 (+305.88%)
KaryoploterkaryoploteR - An R/Bioconductor package to plot arbitrary data along the genome
Stars: ✭ 192 (+464.71%)
GenometoolsGenomeTools genome analysis system.
Stars: ✭ 186 (+447.06%)
IntermineA powerful open source data warehouse system
Stars: ✭ 195 (+473.53%)
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 (+297.06%)
BowtieAn ultrafast memory-efficient short read aligner
Stars: ✭ 221 (+550%)
MiniasmUltrafast de novo assembly for long noisy reads (though having no consensus step)
Stars: ✭ 216 (+535.29%)
BiopythonOfficial git repository for Biopython (originally converted from CVS)
Stars: ✭ 2,936 (+8535.29%)
Bedops🔬 BEDOPS: high-performance genomic feature operations
Stars: ✭ 215 (+532.35%)
BwaBurrow-Wheeler Aligner for short-read alignment (see minimap2 for long-read alignment)
Stars: ✭ 970 (+2752.94%)
GatkOfficial code repository for GATK versions 4 and up
Stars: ✭ 1,002 (+2847.06%)
HifiasmHifiasm: a haplotype-resolved assembler for accurate Hifi reads
Stars: ✭ 134 (+294.12%)
MinigraphProof-of-concept seq-to-graph mapper and graph generator
Stars: ✭ 206 (+505.88%)
Hap.pyHaplotype VCF comparison tools
Stars: ✭ 249 (+632.35%)