staramrScans genome contigs against the ResFinder, PlasmidFinder, and PointFinder databases.
Stars: ✭ 52 (-36.59%)
Bio.jl[DEPRECATED] Bioinformatics and Computational Biology Infrastructure for Julia
Stars: ✭ 257 (+213.41%)
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 (-76.83%)
PostguiA React web application to query and share any PostgreSQL database.
Stars: ✭ 260 (+217.07%)
plasmidtronAssembling the cause of phenotypes and genotypes from NGS data
Stars: ✭ 27 (-67.07%)
BioBioinformatics library for .NET
Stars: ✭ 90 (+9.76%)
SmudgeplotInference of ploidy and heterozygosity structure using whole genome sequencing data
Stars: ✭ 98 (+19.51%)
bacnetBACNET is a Java based platform to develop website for multi-omics analysis
Stars: ✭ 12 (-85.37%)
CoolerA cool place to store your Hi-C
Stars: ✭ 112 (+36.59%)
CgrangesA C/C++ library for fast interval overlap queries (with a "bedtools coverage" example)
Stars: ✭ 111 (+35.37%)
bystroBystro genetic analysis (annotation, filtering, statistics)
Stars: ✭ 31 (-62.2%)
Somalierfast sample-swap and relatedness checks on BAMs/CRAMs/VCFs/GVCFs... "like damn that is one smart wine guy"
Stars: ✭ 128 (+56.1%)
SarekDetect germline or somatic variants from normal or tumour/normal whole-genome or targeted sequencing
Stars: ✭ 124 (+51.22%)
OctopusBayesian haplotype-based mutation calling
Stars: ✭ 131 (+59.76%)
Kmer CntCode examples of fast and simple k-mer counters for tutorial purposes
Stars: ✭ 124 (+51.22%)
HgvsPython library to parse, format, validate, normalize, and map sequence variants. `pip install hgvs`
Stars: ✭ 138 (+68.29%)
WgsimReads simulator
Stars: ✭ 178 (+117.07%)
CirclatorA tool to circularize genome assemblies
Stars: ✭ 121 (+47.56%)
GenometoolsGenomeTools genome analysis system.
Stars: ✭ 186 (+126.83%)
RibbonA genome browser that shows long reads and complex variants better
Stars: ✭ 184 (+124.39%)
GalaxyData intensive science for everyone.
Stars: ✭ 812 (+890.24%)
Janggu Deep learning infrastructure for bioinformatics
Stars: ✭ 174 (+112.2%)
MiniasmUltrafast de novo assembly for long noisy reads (though having no consensus step)
Stars: ✭ 216 (+163.41%)
Bedops🔬 BEDOPS: high-performance genomic feature operations
Stars: ✭ 215 (+162.2%)
HailScalable genomic data analysis.
Stars: ✭ 706 (+760.98%)
faster lmm dA faster lmm for GWAS. Supports GPU backend.
Stars: ✭ 12 (-85.37%)
jgi-queryA simple command-line tool to download data from Joint Genome Institute databases
Stars: ✭ 38 (-53.66%)
wgs2ncbiToolkit for preparing genomes for submission to NCBI
Stars: ✭ 25 (-69.51%)
Hap.pyHaplotype VCF comparison tools
Stars: ✭ 249 (+203.66%)
simplesamSimple pure Python SAM parser and objects for working with SAM records
Stars: ✭ 50 (-39.02%)
wdlRunRElastic, reproducible, and reusable genomic data science tools from R backed by cloud resources
Stars: ✭ 34 (-58.54%)
catchA package for designing compact and comprehensive capture probe sets.
Stars: ✭ 55 (-32.93%)
CanvasxpressJavaScript VisualizationTools
Stars: ✭ 247 (+201.22%)
Cyvcf2cython + htslib == fast VCF and BCF processing
Stars: ✭ 243 (+196.34%)
EarlGreyEarl Grey: A fully automated TE curation and annotation pipeline
Stars: ✭ 25 (-69.51%)
Gwa tutorialA comprehensive tutorial about GWAS and PRS
Stars: ✭ 303 (+269.51%)
Bowtie2A fast and sensitive gapped read aligner
Stars: ✭ 365 (+345.12%)
JcviPython library to facilitate genome assembly, annotation, and comparative genomics
Stars: ✭ 404 (+392.68%)
Sixess🔬🐛 Rapid 16s rRNA identification from isolate FASTQ files
Stars: ✭ 14 (-82.93%)
Awesome Expression Browser😎 A curated list of software and resources for exploring and visualizing (browsing) expression data 😎
Stars: ✭ 72 (-12.2%)
GenozipCompressor for genomic files (FASTQ, SAM/BAM, VCF, FASTA, GVF, 23andMe...), up to 5x better than gzip and faster too
Stars: ✭ 53 (-35.37%)
Uncurl pythonUNCURL is a tool for single cell RNA-seq data analysis.
Stars: ✭ 13 (-84.15%)
ScanpySingle-Cell Analysis in Python. Scales to >1M cells.
Stars: ✭ 858 (+946.34%)
Sv2Support Vector Structural Variation Genotyper
Stars: ✭ 52 (-36.59%)
ScispacyA full spaCy pipeline and models for scientific/biomedical documents.
Stars: ✭ 855 (+942.68%)
NonpareilEstimate metagenomic coverage and sequence diversity
Stars: ✭ 26 (-68.29%)
GlobalbioticinteractionsGlobal Biotic Interactions provides access to existing species interaction datasets
Stars: ✭ 71 (-13.41%)
EmperorEmperor a tool for the analysis and visualization of large microbial ecology datasets
Stars: ✭ 51 (-37.8%)
Taxadb🐣 locally query the ncbi taxonomy
Stars: ✭ 26 (-68.29%)
PretzelJavascript full-stack framework for Big Data visualisation and analysis
Stars: ✭ 26 (-68.29%)
AioliFramework for building fast genomics web tools with WebAssembly and WebWorkers
Stars: ✭ 51 (-37.8%)
16gtSimultaneous detection of SNPs and Indels using a 16-genotype probabilistic model
Stars: ✭ 26 (-68.29%)
Bcalmcompacted de Bruijn graph construction in low memory
Stars: ✭ 69 (-15.85%)
YacrdYet Another Chimeric Read Detector
Stars: ✭ 49 (-40.24%)
Metacachememory efficient, fast & precise taxnomomic classification system for metagenomic read mapping
Stars: ✭ 26 (-68.29%)