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echolocatoRAutomated statistical and functional fine-mapping pipeline with extensive API access to datasets.
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prostoProsto is a data processing toolkit radically changing how data is processed by heavily relying on functions and operations with functions - an alternative to map-reduce and join-groupby
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mviewMView extracts and reformats the results of a sequence database search or multiple alignment.
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CATTAn ultra-sensitive and precise tool for characterizing T cell CDR3 sequences in TCR-seq and RNA-seq data.
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faster lmm dA faster lmm for GWAS. Supports GPU backend.
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geneviewGenomics data visualization in Python by using matplotlib.
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machine-learning-data-pipelinePipeline module for parallel real-time data processing for machine learning models development and production purposes.
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PHATPathogen-Host Analysis Tool - A modern Next-Generation Sequencing (NGS) analysis platform
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saffrontreeSaffronTree: Reference free rapid phylogenetic tree construction from raw read data
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calN50Compute N50/NG50 and auN/auNG
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go4bioGolang for Bioinformatics
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MetaOmGraphMetaOmGraph: a workbench for interactive exploratory data analysis of large expression datasets
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staramrScans genome contigs against the ResFinder, PlasmidFinder, and PointFinder databases.
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biolink-apiAPI for linked biological knowledge
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dna-sculpture3D printed sculpture of a DNA molecule, showing my own genome
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RNArtistCoreA Kotlin DSL and library to create and plot RNA 2D structures
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CENTIPEDE.tutorial🐛 How to use CENTIPEDE to determine if a transcription factor is bound.
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wdlRunRElastic, reproducible, and reusable genomic data science tools from R backed by cloud resources
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pyrpipeReproducible bioinformatics pipelines in python. Import any Unix tool/command in python.
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imputationserverMichigan Imputation Server: A new web-based service for imputation that facilitates access to new reference panels and greatly improves user experience and productivity
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orfipyFast and flexible ORF finder
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hotmapWebGL Heatmap Viewer for Big Data and Bioinformatics
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NeuroSEEDImplementation of Neural Distance Embeddings for Biological Sequences (NeuroSEED) in PyTorch (NeurIPS 2021)
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slamdunkStreamlining SLAM-seq analysis with ultra-high sensitivity
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CAFE5Version 5 of the CAFE phylogenetics software
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atroposAn NGS read trimming tool that is specific, sensitive, and speedy. (production)
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mulledMulled - Automatized Containerized Software Repository
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dnaioRead and write FASTQ and FASTA efficiently from Python
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vcf2gwasPython API for comprehensive GWAS analysis using GEMMA
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ntHashFast hash function for DNA sequences
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companionThis repository has been archived, currently maintained version is at https://github.com/iii-companion/companion
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OpenGene.jl(No maintenance) OpenGene, core libraries for NGS data analysis and bioinformatics in Julia
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simplesamSimple pure Python SAM parser and objects for working with SAM records
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Market-Mix-ModelingMarket Mix Modelling for an eCommerce firm to estimate the impact of various marketing levers on sales
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klar-EDAA python library for automated exploratory data analysis
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awesome-small-molecule-mlA curated list of resources for machine learning for small-molecule drug discovery
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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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referenceseekerRapid determination of appropriate reference genomes.
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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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S-PCGCHeritability, genetic correlation and functional enrichment estimation for case-control studies
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adjclustAdjacency-constrained hierarchical clustering of a similarity matrix
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bystroBystro genetic analysis (annotation, filtering, statistics)
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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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admixrAn R package for reproducible and automated ADMIXTOOLS analyses
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codon-usage-tables📊 Codon usage tables in code-friendly format + Python bindings
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BioDiscMLLarge-scale automatic feature selection for biomarker discovery in high-dimensional OMICs data
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paccmann datasetspytoda - PaccMann PyTorch Dataset Classes. Read the docs: https://paccmann.github.io/paccmann_datasets/
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gene-oracleFeature extraction algorithm for genomic data
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rkmhClassify sequencing reads using MinHash.
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sparklanesA lightweight data processing framework for Apache Spark
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catchA package for designing compact and comprehensive capture probe sets.
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siriusSIRIUS is a software for discovering a landscape of de-novo identification of metabolites using tandem mass spectrometry. This repository contains the code of the SIRIUS Software (GUI and CLI)
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CeleScopeSingle Cell Analysis Pipelines
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biskitA Python platform for Structural Bioinformatics
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tftargets🎯 Human transcription factor target genes.
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GRAFIMOGRAph-based Finding of Individual Motif Occurrences
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