ScoaryPan-genome wide association studies
SvtyperBayesian genotyper for structural variants
SibeliazA fast whole-genome aligner based on de Bruijn graphs
Fastq.bioAn interactive web tool for quality control of DNA sequencing data
BgtFlexible genotype query among 30,000+ samples whole-genome
GubbinsRapid phylogenetic analysis of large samples of recombinant bacterial whole genome sequences using Gubbins
BluegenesA friendly next-generation interface for Genomic data discovery powered by InterMine
Deep ReviewA collaboratively written review paper on deep learning, genomics, and precision medicine
Dna NnModel and predict short DNA sequence features with neural networks
MixomicsDevelopment repository for the Bioconductor package 'mixOmics '
GenozipCompressor for genomic files (FASTQ, SAM/BAM, VCF, FASTA, GVF, 23andMe...), up to 5x better than gzip and faster too
AioliFramework for building fast genomics web tools with WebAssembly and WebWorkers
DramDistilled and Refined Annotation of Metabolism: A tool for the annotation and curation of function for microbial and viral genomes
Quota AlignmentGuided synteny alignment between duplicated genomes (within specified quota constraint)
SnsAnalysis pipelines for sequencing data
Jigvigv.js server and automatic configuration to view bam/cram/vcf/bed. "working in under 1 minute"
GatkOfficial code repository for GATK versions 4 and up
RadiatorRADseq Data Exploration, Manipulation and Visualization using R
BwaBurrow-Wheeler Aligner for short-read alignment (see minimap2 for long-read alignment)
Minimap2A versatile pairwise aligner for genomic and spliced nucleotide sequences
Sixess🔬🐛 Rapid 16s rRNA identification from isolate FASTQ files
Tiledb VcfEfficient variant-call data storage and retrieval library using the TileDB storage library.
BgdataA Suite of Packages for Analysis of Big Genomic Data
GalaxyData intensive science for everyone.
Vgtools for working with genome variation graphs
HailScalable genomic data analysis.
NucleusPython and C++ code for reading and writing genomics data.
DeeptoolsTools to process and analyze deep sequencing data.
Biojava📖🔬☕️ BioJava is an open-source project dedicated to providing a Java library for processing biological data.
GoatoolsPython library to handle Gene Ontology (GO) terms
Vcflib C++ library and cmdline tools for parsing and manipulating VCF files
JcviPython library to facilitate genome assembly, annotation, and comparative genomics
JbrowseA modern genome browser built with JavaScript and HTML5.
Bowtie2A fast and sensitive gapped read aligner
MegahitUltra-fast and memory-efficient (meta-)genome assembler
JvarkitJava utilities for Bioinformatics
PyfaidxEfficient pythonic random access to fasta subsequences
ArvadosAn open source platform for managing and analyzing biomedical big data
SeqA high-performance, Pythonic language for bioinformatics
PygenoPersonalized Genomics and Proteomics. Main diet: Ensembl, side dishes: SNPs
PostguiA React web application to query and share any PostgreSQL database.
Vcfannoannotate a VCF with other VCFs/BEDs/tabixed files
Bio.jl[DEPRECATED] Bioinformatics and Computational Biology Infrastructure for Julia
Eggnog MapperFast genome-wide functional annotation through orthology assignment
PHANOTATEPHANOTATE: a tool to annotate phage genomes.
gff3toemblConverts Prokka GFF3 files to EMBL files for uploading annotated assemblies to EBI
mccortexDe novo genome assembly and multisample variant calling
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.
fermikitDe novo assembly based variant calling pipeline for Illumina short reads
bacnetBACNET is a Java based platform to develop website for multi-omics analysis
EarlGreyEarl Grey: A fully automated TE curation and annotation pipeline
dna-traitsA fast 23andMe genome text file parser, now superseded by arv