saffrontreeSaffronTree: Reference free rapid phylogenetic tree construction from raw read data
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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
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plasmidtronAssembling the cause of phenotypes and genotypes from NGS data
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AribaAntimicrobial Resistance Identification By Assembly
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RoaryRapid large-scale prokaryote pan genome analysis
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mlst checkMultilocus sequence typing by blast using the schemes from PubMLST
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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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tiptoftPredict plasmids from uncorrected long read data
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GalaxyData intensive science for everyone.
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HgvsPython library to parse, format, validate, normalize, and map sequence variants. `pip install hgvs`
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assembly improvementImprove the quality of a denovo assembly by scaffolding and gap filling
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SnsAnalysis pipelines for sequencing data
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ntHashFast hash function for DNA sequences
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calN50Compute N50/NG50 and auN/auNG
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staramrScans genome contigs against the ResFinder, PlasmidFinder, and PointFinder databases.
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bystroBystro genetic analysis (annotation, filtering, statistics)
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chromapFast alignment and preprocessing of chromatin profiles
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companionThis repository has been archived, currently maintained version is at https://github.com/iii-companion/companion
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simplesamSimple pure Python SAM parser and objects for working with SAM records
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wdlRunRElastic, reproducible, and reusable genomic data science tools from R backed by cloud resources
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gencoreGenerate duplex/single consensus reads to reduce sequencing noises and remove duplications
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dna-traitsA fast 23andMe genome text file parser, now superseded by arv
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MigmapHTS-compatible wrapper for IgBlast V-(D)-J mapping tool
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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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Vcfannoannotate a VCF with other VCFs/BEDs/tabixed files
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dysgudysgu-SV is a collection of tools for calling structural variants using short or long reads
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netSmoothnetSmooth: A Network smoothing based method for Single Cell RNA-seq imputation
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fermikitDe novo assembly based variant calling pipeline for Illumina short reads
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Bio.jl[DEPRECATED] Bioinformatics and Computational Biology Infrastructure for Julia
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PostguiA React web application to query and share any PostgreSQL database.
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PyfaidxEfficient pythonic random access to fasta subsequences
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BwaBurrow-Wheeler Aligner for short-read alignment (see minimap2 for long-read alignment)
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