CirclatorA tool to circularize genome assemblies
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AribaAntimicrobial Resistance Identification By Assembly
Stars: ✭ 96 (-45.45%)
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 (-23.3%)
gff3toemblConverts Prokka GFF3 files to EMBL files for uploading annotated assemblies to EBI
Stars: ✭ 27 (-84.66%)
saffrontreeSaffronTree: Reference free rapid phylogenetic tree construction from raw read data
Stars: ✭ 17 (-90.34%)
GubbinsRapid phylogenetic analysis of large samples of recombinant bacterial whole genome sequences using Gubbins
Stars: ✭ 67 (-61.93%)
plasmidtronAssembling the cause of phenotypes and genotypes from NGS data
Stars: ✭ 27 (-84.66%)
snp-sitesFinds SNP sites from a multi-FASTA alignment file
Stars: ✭ 182 (+3.41%)
GenomicsA collection of scripts and notes related to genomics and bioinformatics
Stars: ✭ 101 (-42.61%)
GalaxyData intensive science for everyone.
Stars: ✭ 812 (+361.36%)
assembly improvementImprove the quality of a denovo assembly by scaffolding and gap filling
Stars: ✭ 46 (-73.86%)
SnsAnalysis pipelines for sequencing data
Stars: ✭ 43 (-75.57%)
GatkOfficial code repository for GATK versions 4 and up
Stars: ✭ 1,002 (+469.32%)
HgvsPython library to parse, format, validate, normalize, and map sequence variants. `pip install hgvs`
Stars: ✭ 138 (-21.59%)
DeepvariantDeepVariant is an analysis pipeline that uses a deep neural network to call genetic variants from next-generation DNA sequencing data.
Stars: ✭ 2,404 (+1265.91%)
Fastq.bioAn interactive web tool for quality control of DNA sequencing data
Stars: ✭ 76 (-56.82%)
mlst checkMultilocus sequence typing by blast using the schemes from PubMLST
Stars: ✭ 22 (-87.5%)
gubbinsRapid phylogenetic analysis of large samples of recombinant bacterial whole genome sequences using Gubbins
Stars: ✭ 103 (-41.48%)
SequenceserverIntuitive local web frontend for the BLAST bioinformatics tool
Stars: ✭ 198 (+12.5%)
catchA package for designing compact and comprehensive capture probe sets.
Stars: ✭ 55 (-68.75%)
tiptoftPredict plasmids from uncorrected long read data
Stars: ✭ 27 (-84.66%)
Bowtie2A fast and sensitive gapped read aligner
Stars: ✭ 365 (+107.39%)
JbrowseA modern genome browser built with JavaScript and HTML5.
Stars: ✭ 393 (+123.3%)
Bwa Mem2The next version of bwa-mem
Stars: ✭ 408 (+131.82%)
MegahitUltra-fast and memory-efficient (meta-)genome assembler
Stars: ✭ 343 (+94.89%)
JvarkitJava utilities for Bioinformatics
Stars: ✭ 313 (+77.84%)
JcviPython library to facilitate genome assembly, annotation, and comparative genomics
Stars: ✭ 404 (+129.55%)
PyfaidxEfficient pythonic random access to fasta subsequences
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DeeptoolsTools to process and analyze deep sequencing data.
Stars: ✭ 448 (+154.55%)
NucleusPython and C++ code for reading and writing genomics data.
Stars: ✭ 657 (+273.3%)
Gwa tutorialA comprehensive tutorial about GWAS and PRS
Stars: ✭ 303 (+72.16%)
Biojava📖🔬☕️ BioJava is an open-source project dedicated to providing a Java library for processing biological data.
Stars: ✭ 434 (+146.59%)
HailScalable genomic data analysis.
Stars: ✭ 706 (+301.14%)
Rnaseq WorkflowA repository for setting up a RNAseq workflow
Stars: ✭ 170 (-3.41%)
Tiledb VcfEfficient variant-call data storage and retrieval library using the TileDB storage library.
Stars: ✭ 26 (-85.23%)
Minimap2A versatile pairwise aligner for genomic and spliced nucleotide sequences
Stars: ✭ 912 (+418.18%)
BwaBurrow-Wheeler Aligner for short-read alignment (see minimap2 for long-read alignment)
Stars: ✭ 970 (+451.14%)
FastpAn ultra-fast all-in-one FASTQ preprocessor (QC/adapters/trimming/filtering/splitting/merging...)
Stars: ✭ 966 (+448.86%)
AfterqcAutomatic Filtering, Trimming, Error Removing and Quality Control for fastq data
Stars: ✭ 169 (-3.98%)
DramDistilled and Refined Annotation of Metabolism: A tool for the annotation and curation of function for microbial and viral genomes
Stars: ✭ 47 (-73.3%)
ArvadosAn open source platform for managing and analyzing biomedical big data
Stars: ✭ 274 (+55.68%)
Helmsmanhighly-efficient & lightweight mutation signature matrix aggregation
Stars: ✭ 19 (-89.2%)
MigmapHTS-compatible wrapper for IgBlast V-(D)-J mapping tool
Stars: ✭ 38 (-78.41%)
Dna NnModel and predict short DNA sequence features with neural networks
Stars: ✭ 59 (-66.48%)
Awesome 10x GenomicsList of tools and resources related to the 10x Genomics GEMCode/Chromium system
Stars: ✭ 82 (-53.41%)
SvtyperBayesian genotyper for structural variants
Stars: ✭ 79 (-55.11%)
TruvariStructural variant toolkit for VCFs
Stars: ✭ 85 (-51.7%)
SibeliazA fast whole-genome aligner based on de Bruijn graphs
Stars: ✭ 76 (-56.82%)
BioBioinformatics library for .NET
Stars: ✭ 90 (-48.86%)
SmudgeplotInference of ploidy and heterozygosity structure using whole genome sequencing data
Stars: ✭ 98 (-44.32%)
CgrangesA C/C++ library for fast interval overlap queries (with a "bedtools coverage" example)
Stars: ✭ 111 (-36.93%)
UgeneUGENE is free open-source cross-platform bioinformatics software
Stars: ✭ 112 (-36.36%)
HicexplorerHiCExplorer is a powerful and easy to use set of tools to process, normalize and visualize Hi-C data.
Stars: ✭ 116 (-34.09%)
HifiasmHifiasm: a haplotype-resolved assembler for accurate Hifi reads
Stars: ✭ 134 (-23.86%)