atroposAn NGS read trimming tool that is specific, sensitive, and speedy. (production)
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simplesamSimple pure Python SAM parser and objects for working with SAM records
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mulledMulled - Automatized Containerized Software Repository
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catchA package for designing compact and comprehensive capture probe sets.
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ntHashFast hash function for DNA sequences
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wdlRunRElastic, reproducible, and reusable genomic data science tools from R backed by cloud resources
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calN50Compute N50/NG50 and auN/auNG
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CoNekTCoNekT (short for Co-expression Network Toolkit) is a platform to browse co-expression data and enable cross-species comparisons.
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Binning refinerImproving genome bins through the combination of different binning programs
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orfipyFast and flexible ORF finder
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ngstoolsMy own tools code for NGS data analysis (Next Generation Sequencing)
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dnaioRead and write FASTQ and FASTA efficiently from Python
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biskitA Python platform for Structural Bioinformatics
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GenomicDataCommonsProvide R access to the NCI Genomic Data Commons portal.
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CASECyber-investigation Analysis Standard Expression (CASE) Ontology
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sirene-ldTransformation du répertoire SIRENE (CSV) au format RDF pour publication en Linked Data
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pyrpipeReproducible bioinformatics pipelines in python. Import any Unix tool/command in python.
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verifiable-dataOpen Source Decentralized Identifiers and Verifiable Credentials Infrastructure and Tooling
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cubiqlCubiQL: A GraphQL service for querying multidimensional Linked Data Cubes
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CENTIPEDE.tutorial🐛 How to use CENTIPEDE to determine if a transcription factor is bound.
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CAFE5Version 5 of the CAFE phylogenetics software
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admixrAn R package for reproducible and automated ADMIXTOOLS analyses
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gene-oracleFeature extraction algorithm for genomic data
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SumStatsRehabGWAS summary statistics files QC tool
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tftargets🎯 Human transcription factor target genes.
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bystroBystro genetic analysis (annotation, filtering, statistics)
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nPhasePloidy agnostic phasing pipeline and algorithm
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plasmidtronAssembling the cause of phenotypes and genotypes from NGS data
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MetaOmGraphMetaOmGraph: a workbench for interactive exploratory data analysis of large expression datasets
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saffrontreeSaffronTree: Reference free rapid phylogenetic tree construction from raw read data
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referenceseekerRapid determination of appropriate reference genomes.
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biolink-apiAPI for linked biological knowledge
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SVCollectorMethod to optimally select samples for validation and resequencing
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go4bioGolang for Bioinformatics
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rdf-ldpA suite of LDP software and middleware for RDF.rb & Rack
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RNArtistCoreA Kotlin DSL and library to create and plot RNA 2D structures
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staramrScans genome contigs against the ResFinder, PlasmidFinder, and PointFinder databases.
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OpenGene.jl(No maintenance) OpenGene, core libraries for NGS data analysis and bioinformatics in Julia
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companionThis repository has been archived, currently maintained version is at https://github.com/iii-companion/companion
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tibannaTibanna helps you run your genomic pipelines on Amazon cloud (AWS). It is used by the 4DN DCIC (4D Nucleome Data Coordination and Integration Center) to process data. Tibanna supports CWL/WDL (w/ docker), Snakemake (w/ conda) and custom Docker/shell command.
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StackedDAEStacked Denoising AutoEncoder based on TensorFlow
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hotsubCommand line tool to run batch jobs concurrently with ETL framework on AWS or other cloud computing resources
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mviewMView extracts and reformats the results of a sequence database search or multiple alignment.
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slamdunkStreamlining SLAM-seq analysis with ultra-high sensitivity
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awesome-small-molecule-mlA curated list of resources for machine learning for small-molecule drug discovery
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flexidotHighly customizable, ambiguity-aware dotplots for visual sequence analyses
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ccsCCS: Generate Highly Accurate Single-Molecule Consensus Reads (HiFi Reads)
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bio toolsUseful bioinformatic scripts
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hotmapWebGL Heatmap Viewer for Big Data and Bioinformatics
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