JvarkitJava utilities for Bioinformatics
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PygenoPersonalized Genomics and Proteomics. Main diet: Ensembl, side dishes: SNPs
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Deep RulesTen Quick Tips for Deep Learning in Biology
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IntermineA powerful open source data warehouse system
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Bio.jl[DEPRECATED] Bioinformatics and Computational Biology Infrastructure for Julia
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Hap.pyHaplotype VCF comparison tools
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jgi-queryA simple command-line tool to download data from Joint Genome Institute databases
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gff3toemblConverts Prokka GFF3 files to EMBL files for uploading annotated assemblies to EBI
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Bedops🔬 BEDOPS: high-performance genomic feature operations
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MiniasmUltrafast de novo assembly for long noisy reads (though having no consensus step)
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CanvasxpressJavaScript VisualizationTools
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BowtieAn ultrafast memory-efficient short read aligner
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ArvadosAn open source platform for managing and analyzing biomedical big data
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dysgudysgu-SV is a collection of tools for calling structural variants using short or long reads
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faster lmm dA faster lmm for GWAS. Supports GPU backend.
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saffrontreeSaffronTree: Reference free rapid phylogenetic tree construction from raw read data
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wdlRunRElastic, reproducible, and reusable genomic data science tools from R backed by cloud resources
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catchA package for designing compact and comprehensive capture probe sets.
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MegahitUltra-fast and memory-efficient (meta-)genome assembler
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GenomicDataCommonsProvide R access to the NCI Genomic Data Commons portal.
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plasmidtronAssembling the cause of phenotypes and genotypes from NGS data
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SeqA high-performance, Pythonic language for bioinformatics
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lexicon-mono-seqDOM Text Based Multiple Sequence Alignment Library
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MinigraphProof-of-concept seq-to-graph mapper and graph generator
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SequenceserverIntuitive local web frontend for the BLAST bioinformatics tool
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TdcTherapeutics Data Commons: Machine Learning Datasets and Tasks for Therapeutics
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reg-genRegulatory Genomics Toolbox: Python library and set of tools for the integrative analysis of high throughput regulatory genomics data.
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netSmoothnetSmooth: A Network smoothing based method for Single Cell RNA-seq imputation
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PostguiA React web application to query and share any PostgreSQL database.
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BiopythonOfficial git repository for Biopython (originally converted from CVS)
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Cyvcf2cython + htslib == fast VCF and BCF processing
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macrelPredict AMPs in (meta)genomes and peptides
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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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unimapA EXPERIMENTAL fork of minimap2 optimized for assembly-to-reference alignment
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wgs2ncbiToolkit for preparing genomes for submission to NCBI
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Scaff10XPipeline for scaffolding and breaking a genome assembly using 10x genomics linked-reads
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ntHashFast hash function for DNA sequences
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simplesamSimple pure Python SAM parser and objects for working with SAM records
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calN50Compute N50/NG50 and auN/auNG
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GenometoolsGenomeTools genome analysis system.
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FALDOFeature Annotation Location Description Ontology
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flexidotHighly customizable, ambiguity-aware dotplots for visual sequence analyses
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bystroBystro genetic analysis (annotation, filtering, statistics)
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Vcfannoannotate a VCF with other VCFs/BEDs/tabixed files
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chromapFast alignment and preprocessing of chromatin profiles
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PyfaidxEfficient pythonic random access to fasta subsequences
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staramrScans genome contigs against the ResFinder, PlasmidFinder, and PointFinder databases.
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EarlGreyEarl Grey: A fully automated TE curation and annotation pipeline
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dna-traitsA fast 23andMe genome text file parser, now superseded by arv
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tiptoftPredict plasmids from uncorrected long read data
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Gwa tutorialA comprehensive tutorial about GWAS and PRS
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bacnetBACNET is a Java based platform to develop website for multi-omics analysis
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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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Janggu Deep learning infrastructure for bioinformatics
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RibbonA genome browser that shows long reads and complex variants better
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companionThis repository has been archived, currently maintained version is at https://github.com/iii-companion/companion
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awesome-geneticsA curated list of awesome bioinformatics software.
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