fermikitDe novo assembly based variant calling pipeline for Illumina short reads
Stars: ✭ 98 (-19.01%)
UgeneUGENE is free open-source cross-platform bioinformatics software
Stars: ✭ 112 (-7.44%)
Rnaseq WorkflowA repository for setting up a RNAseq workflow
Stars: ✭ 170 (+40.5%)
AfterqcAutomatic Filtering, Trimming, Error Removing and Quality Control for fastq data
Stars: ✭ 169 (+39.67%)
SvtyperBayesian genotyper for structural variants
Stars: ✭ 79 (-34.71%)
SarekDetect germline or somatic variants from normal or tumour/normal whole-genome or targeted sequencing
Stars: ✭ 124 (+2.48%)
Janggu Deep learning infrastructure for bioinformatics
Stars: ✭ 174 (+43.8%)
Deep RulesTen Quick Tips for Deep Learning in Biology
Stars: ✭ 179 (+47.93%)
PostguiA React web application to query and share any PostgreSQL database.
Stars: ✭ 260 (+114.88%)
PygenoPersonalized Genomics and Proteomics. Main diet: Ensembl, side dishes: SNPs
Stars: ✭ 261 (+115.7%)
Dna NnModel and predict short DNA sequence features with neural networks
Stars: ✭ 59 (-51.24%)
Kmer CntCode examples of fast and simple k-mer counters for tutorial purposes
Stars: ✭ 124 (+2.48%)
JvarkitJava utilities for Bioinformatics
Stars: ✭ 313 (+158.68%)
CanvasxpressJavaScript VisualizationTools
Stars: ✭ 247 (+104.13%)
BiopythonOfficial git repository for Biopython (originally converted from CVS)
Stars: ✭ 2,936 (+2326.45%)
Cyvcf2cython + htslib == fast VCF and BCF processing
Stars: ✭ 243 (+100.83%)
Bowtie2A fast and sensitive gapped read aligner
Stars: ✭ 365 (+201.65%)
ArvadosAn open source platform for managing and analyzing biomedical big data
Stars: ✭ 274 (+126.45%)
MegahitUltra-fast and memory-efficient (meta-)genome assembler
Stars: ✭ 343 (+183.47%)
NglessNGLess: NGS with less work
Stars: ✭ 115 (-4.96%)
BowtieAn ultrafast memory-efficient short read aligner
Stars: ✭ 221 (+82.64%)
unimapA EXPERIMENTAL fork of minimap2 optimized for assembly-to-reference alignment
Stars: ✭ 76 (-37.19%)
wgs2ncbiToolkit for preparing genomes for submission to NCBI
Stars: ✭ 25 (-79.34%)
simplesamSimple pure Python SAM parser and objects for working with SAM records
Stars: ✭ 50 (-58.68%)
Scaff10XPipeline for scaffolding and breaking a genome assembly using 10x genomics linked-reads
Stars: ✭ 21 (-82.64%)
NucleusPython and C++ code for reading and writing genomics data.
Stars: ✭ 657 (+442.98%)
HailScalable genomic data analysis.
Stars: ✭ 706 (+483.47%)
reg-genRegulatory Genomics Toolbox: Python library and set of tools for the integrative analysis of high throughput regulatory genomics data.
Stars: ✭ 64 (-47.11%)
Tiledb VcfEfficient variant-call data storage and retrieval library using the TileDB storage library.
Stars: ✭ 26 (-78.51%)
GenomicDataCommonsProvide R access to the NCI Genomic Data Commons portal.
Stars: ✭ 64 (-47.11%)
Helmsmanhighly-efficient & lightweight mutation signature matrix aggregation
Stars: ✭ 19 (-84.3%)
Minimap2A versatile pairwise aligner for genomic and spliced nucleotide sequences
Stars: ✭ 912 (+653.72%)
BwaBurrow-Wheeler Aligner for short-read alignment (see minimap2 for long-read alignment)
Stars: ✭ 970 (+701.65%)
EarlGreyEarl Grey: A fully automated TE curation and annotation pipeline
Stars: ✭ 25 (-79.34%)
dna-traitsA fast 23andMe genome text file parser, now superseded by arv
Stars: ✭ 64 (-47.11%)
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 (-84.3%)
Vcfannoannotate a VCF with other VCFs/BEDs/tabixed files
Stars: ✭ 259 (+114.05%)
Bio.jl[DEPRECATED] Bioinformatics and Computational Biology Infrastructure for Julia
Stars: ✭ 257 (+112.4%)
SeqA high-performance, Pythonic language for bioinformatics
Stars: ✭ 263 (+117.36%)
PyfaidxEfficient pythonic random access to fasta subsequences
Stars: ✭ 307 (+153.72%)
Gwa tutorialA comprehensive tutorial about GWAS and PRS
Stars: ✭ 303 (+150.41%)
bystroBystro genetic analysis (annotation, filtering, statistics)
Stars: ✭ 31 (-74.38%)
DeeptoolsTools to process and analyze deep sequencing data.
Stars: ✭ 448 (+270.25%)
Biojava📖🔬☕️ BioJava is an open-source project dedicated to providing a Java library for processing biological data.
Stars: ✭ 434 (+258.68%)
Bwa Mem2The next version of bwa-mem
Stars: ✭ 408 (+237.19%)
MigmapHTS-compatible wrapper for IgBlast V-(D)-J mapping tool
Stars: ✭ 38 (-68.6%)
TruvariStructural variant toolkit for VCFs
Stars: ✭ 85 (-29.75%)
FastpAn ultra-fast all-in-one FASTQ preprocessor (QC/adapters/trimming/filtering/splitting/merging...)
Stars: ✭ 966 (+698.35%)
JcviPython library to facilitate genome assembly, annotation, and comparative genomics
Stars: ✭ 404 (+233.88%)
staramrScans genome contigs against the ResFinder, PlasmidFinder, and PointFinder databases.
Stars: ✭ 52 (-57.02%)
JbrowseA modern genome browser built with JavaScript and HTML5.
Stars: ✭ 393 (+224.79%)
DramDistilled and Refined Annotation of Metabolism: A tool for the annotation and curation of function for microbial and viral genomes
Stars: ✭ 47 (-61.16%)
HicexplorerHiCExplorer is a powerful and easy to use set of tools to process, normalize and visualize Hi-C data.
Stars: ✭ 116 (-4.13%)
PymzmlpymzML - an interface between Python and mzML Mass spectrometry Files
Stars: ✭ 100 (-17.36%)