GenomicsA collection of scripts and notes related to genomics and bioinformatics
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GalaxyData intensive science for everyone.
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catchA package for designing compact and comprehensive capture probe sets.
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GatkOfficial code repository for GATK versions 4 and up
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awesome-geneticsA curated list of awesome bioinformatics software.
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dna-traitsA fast 23andMe genome text file parser, now superseded by arv
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Bio.jl[DEPRECATED] Bioinformatics and Computational Biology Infrastructure for Julia
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PyfaidxEfficient pythonic random access to fasta subsequences
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BiopythonOfficial git repository for Biopython (originally converted from CVS)
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SnsAnalysis pipelines for sequencing data
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DeepvariantDeepVariant is an analysis pipeline that uses a deep neural network to call genetic variants from next-generation DNA sequencing data.
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variantkeyNumerical Encoding for Human Genetic Variants
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STingUltrafast sequence typing and gene detection from NGS raw reads
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Biojava📖🔬☕️ BioJava is an open-source project dedicated to providing a Java library for processing biological data.
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Scaff10XPipeline for scaffolding and breaking a genome assembly using 10x genomics linked-reads
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jgi-queryA simple command-line tool to download data from Joint Genome Institute databases
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PHATPathogen-Host Analysis Tool - A modern Next-Generation Sequencing (NGS) analysis platform
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wgs2ncbiToolkit for preparing genomes for submission to NCBI
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simplesamSimple pure Python SAM parser and objects for working with SAM records
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ntHashFast hash function for DNA sequences
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saffrontreeSaffronTree: Reference free rapid phylogenetic tree construction from raw read data
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bystroBystro genetic analysis (annotation, filtering, statistics)
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unimapA EXPERIMENTAL fork of minimap2 optimized for assembly-to-reference alignment
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calN50Compute N50/NG50 and auN/auNG
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orfipyFast and flexible ORF finder
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Bwa Mem2The next version of bwa-mem
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sequenceworkprograms and scripts, mainly python, for analyses related to nucleic or protein sequences
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Hap.pyHaplotype VCF comparison tools
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adaptA package for designing activity-informed nucleic acid diagnostics for viruses.
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CanvasxpressJavaScript VisualizationTools
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JvarkitJava utilities for Bioinformatics
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faster lmm dA faster lmm for GWAS. Supports GPU backend.
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JcviPython library to facilitate genome assembly, annotation, and comparative genomics
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JbrowseA modern genome browser built with JavaScript and HTML5.
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PygenoPersonalized Genomics and Proteomics. Main diet: Ensembl, side dishes: SNPs
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Gwa tutorialA comprehensive tutorial about GWAS and PRS
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wdlRunRElastic, reproducible, and reusable genomic data science tools from R backed by cloud resources
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dysgudysgu-SV is a collection of tools for calling structural variants using short or long reads
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staramrScans genome contigs against the ResFinder, PlasmidFinder, and PointFinder databases.
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companionThis repository has been archived, currently maintained version is at https://github.com/iii-companion/companion
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ArvadosAn open source platform for managing and analyzing biomedical big data
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Cyvcf2cython + htslib == fast VCF and BCF processing
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DeeptoolsTools to process and analyze deep sequencing data.
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reg-genRegulatory Genomics Toolbox: Python library and set of tools for the integrative analysis of high throughput regulatory genomics data.
Stars: ✭ 64 (-90.26%)
SeqA high-performance, Pythonic language for bioinformatics
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plasmidtronAssembling the cause of phenotypes and genotypes from NGS data
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Bowtie2A fast and sensitive gapped read aligner
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PostguiA React web application to query and share any PostgreSQL database.
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Vcfannoannotate a VCF with other VCFs/BEDs/tabixed files
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GenomicDataCommonsProvide R access to the NCI Genomic Data Commons portal.
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chromapFast alignment and preprocessing of chromatin profiles
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netSmoothnetSmooth: A Network smoothing based method for Single Cell RNA-seq imputation
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bacnetBACNET is a Java based platform to develop website for multi-omics analysis
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EarlGreyEarl Grey: A fully automated TE curation and annotation pipeline
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fermikitDe novo assembly based variant calling pipeline for Illumina short reads
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gff3toemblConverts Prokka GFF3 files to EMBL files for uploading annotated assemblies to EBI
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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.
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MegahitUltra-fast and memory-efficient (meta-)genome assembler
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MiniasmUltrafast de novo assembly for long noisy reads (though having no consensus step)
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