Viral NgsViral genomics analysis pipelines
Stars: ✭ 150 (-27.88%)
BwaBurrow-Wheeler Aligner for short-read alignment (see minimap2 for long-read alignment)
Stars: ✭ 970 (+366.35%)
QqmanAn R package for creating Q-Q and manhattan plots from GWAS results
Stars: ✭ 115 (-44.71%)
RibbonA genome browser that shows long reads and complex variants better
Stars: ✭ 184 (-11.54%)
Tiledb VcfEfficient variant-call data storage and retrieval library using the TileDB storage library.
Stars: ✭ 26 (-87.5%)
CgrangesA C/C++ library for fast interval overlap queries (with a "bedtools coverage" example)
Stars: ✭ 111 (-46.63%)
BgdataA Suite of Packages for Analysis of Big Genomic Data
Stars: ✭ 19 (-90.87%)
Smoovestructural variant calling and genotyping with existing tools, but, smoothly.
Stars: ✭ 147 (-29.33%)
Vgtools for working with genome variation graphs
Stars: ✭ 710 (+241.35%)
MsprimeSimulate genealogical trees and genomic sequence data using population genetic models
Stars: ✭ 103 (-50.48%)
NucleusPython and C++ code for reading and writing genomics data.
Stars: ✭ 657 (+215.87%)
SequenceserverIntuitive local web frontend for the BLAST bioinformatics tool
Stars: ✭ 198 (-4.81%)
DeeptoolsTools to process and analyze deep sequencing data.
Stars: ✭ 448 (+115.38%)
SmudgeplotInference of ploidy and heterozygosity structure using whole genome sequencing data
Stars: ✭ 98 (-52.88%)
GoatoolsPython library to handle Gene Ontology (GO) terms
Stars: ✭ 415 (+99.52%)
Bwa Mem2The next version of bwa-mem
Stars: ✭ 408 (+96.15%)
JbrowseA modern genome browser built with JavaScript and HTML5.
Stars: ✭ 393 (+88.94%)
Janggu Deep learning infrastructure for bioinformatics
Stars: ✭ 174 (-16.35%)
MegahitUltra-fast and memory-efficient (meta-)genome assembler
Stars: ✭ 343 (+64.9%)
BioBioinformatics library for .NET
Stars: ✭ 90 (-56.73%)
PyfaidxEfficient pythonic random access to fasta subsequences
Stars: ✭ 307 (+47.6%)
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 (-35.1%)
ArvadosAn open source platform for managing and analyzing biomedical big data
Stars: ✭ 274 (+31.73%)
DkmDynamic Kernel Matching (DKM) for Classifying Data with Non-conforming Features
Stars: ✭ 86 (-58.65%)
PygenoPersonalized Genomics and Proteomics. Main diet: Ensembl, side dishes: SNPs
Stars: ✭ 261 (+25.48%)
MinigraphProof-of-concept seq-to-graph mapper and graph generator
Stars: ✭ 206 (-0.96%)
Vcfannoannotate a VCF with other VCFs/BEDs/tabixed files
Stars: ✭ 259 (+24.52%)
Awesome 10x GenomicsList of tools and resources related to the 10x Genomics GEMCode/Chromium system
Stars: ✭ 82 (-60.58%)
Eggnog MapperFast genome-wide functional annotation through orthology assignment
Stars: ✭ 256 (+23.08%)
OctopusBayesian haplotype-based mutation calling
Stars: ✭ 131 (-37.02%)
SvtyperBayesian genotyper for structural variants
Stars: ✭ 79 (-62.02%)
gff3toemblConverts Prokka GFF3 files to EMBL files for uploading annotated assemblies to EBI
Stars: ✭ 27 (-87.02%)
WgsimReads simulator
Stars: ✭ 178 (-14.42%)
GenomeAnalysisModuleWelcome to the website and github repository for the Genome Analysis Module. This website will guide the learning experience for trainees in the UBC MSc Genetic Counselling Training Program, as they embark on a journey to learn about analyzing genomes.
Stars: ✭ 19 (-90.87%)
Fastq.bioAn interactive web tool for quality control of DNA sequencing data
Stars: ✭ 76 (-63.46%)
bacnetBACNET is a Java based platform to develop website for multi-omics analysis
Stars: ✭ 12 (-94.23%)
Miso LimsMISO: An open-source LIMS for NGS sequencing centres
Stars: ✭ 131 (-37.02%)
dna-traitsA fast 23andMe genome text file parser, now superseded by arv
Stars: ✭ 64 (-69.23%)
GubbinsRapid phylogenetic analysis of large samples of recombinant bacterial whole genome sequences using Gubbins
Stars: ✭ 67 (-67.79%)
tiptoftPredict plasmids from uncorrected long read data
Stars: ✭ 27 (-87.02%)
DeepvariantDeepVariant is an analysis pipeline that uses a deep neural network to call genetic variants from next-generation DNA sequencing data.
Stars: ✭ 2,404 (+1055.77%)
mcscanCommand-line program to wrap dagchainer and combine pairwise results into multi-alignments in column format
Stars: ✭ 18 (-91.35%)
Deep ReviewA collaboratively written review paper on deep learning, genomics, and precision medicine
Stars: ✭ 1,141 (+448.56%)
MAGMA CelltypingFind causal cell-types underlying complex trait genetics
Stars: ✭ 41 (-80.29%)
Somalierfast sample-swap and relatedness checks on BAMs/CRAMs/VCFs/GVCFs... "like damn that is one smart wine guy"
Stars: ✭ 128 (-38.46%)
MixomicsDevelopment repository for the Bioconductor package 'mixOmics '
Stars: ✭ 58 (-72.12%)
awesome-geneticsA curated list of awesome bioinformatics software.
Stars: ✭ 60 (-71.15%)
Goleftgoleft is a collection of bioinformatics tools distributed under MIT license in a single static binary
Stars: ✭ 175 (-15.87%)
AioliFramework for building fast genomics web tools with WebAssembly and WebWorkers
Stars: ✭ 51 (-75.48%)
FlowcraftFlowCraft: a component-based pipeline composer for omics analysis using Nextflow. 🐳📦
Stars: ✭ 208 (+0%)
JuicerA One-Click System for Analyzing Loop-Resolution Hi-C Experiments
Stars: ✭ 203 (-2.4%)
GenometoolsGenomeTools genome analysis system.
Stars: ✭ 186 (-10.58%)
GlowAn open-source toolkit for large-scale genomic analysis
Stars: ✭ 159 (-23.56%)
CirclatorA tool to circularize genome assemblies
Stars: ✭ 121 (-41.83%)
SnsAnalysis pipelines for sequencing data
Stars: ✭ 43 (-79.33%)