IsobarA Python library for creating and manipulating musical patterns, designed for use in algorithmic composition, generative music and sonification. Can be used to generate MIDI events, MIDI files, OSC messages, or custom events.
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AfterqcAutomatic Filtering, Trimming, Error Removing and Quality Control for fastq data
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deMLMaximum likelihood demultiplexing
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HLAxHLA: Fast and accurate HLA typing from short read sequence data
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Beet.jsPolyrhythmic Sequencer library for Web Audio API.
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geneticalgorithm2Supported highly optimized and flexible genetic algorithm package for python
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ShastaDe novo assembly from Oxford Nanopore reads.
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bxtoolsTools for analyzing 10X Genomics data
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UgeneUGENE is free open-source cross-platform bioinformatics software
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Drowsy💤🖌️ AI making tiny Bitsy video games. Features an experimental generative structure inspired by GANs and Genetic Algorithms
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ruck🧬 Modularised Evolutionary Algorithms For Python with Optional JIT and Multiprocessing (Ray) support. Inspired by PyTorch Lightning
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GubbinsRapid phylogenetic analysis of large samples of recombinant bacterial whole genome sequences using Gubbins
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vitaVita - Genetic Programming Framework
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Optimized-MDVRP"Using Genetic Algorithms for Multi-depot Vehicle Routing" paper implementation.
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SequenceserverIntuitive local web frontend for the BLAST bioinformatics tool
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ginkgoCloud-based single-cell copy-number variation analysis tool
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RoaryRapid large-scale prokaryote pan genome analysis
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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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ANCOMBCDifferential abundance (DA) and correlation analyses for microbial absolute abundance data
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AribaAntimicrobial Resistance Identification By Assembly
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desh-dataSequence lineage information extracted from RKI sequence data repo
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Fastq.bioAn interactive web tool for quality control of DNA sequencing data
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snp-sitesFinds SNP sites from a multi-FASTA alignment file
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cacaoCallable Cancer Loci - assessment of sequencing coverage for actionable and pathogenic loci in cancer
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SnsAnalysis pipelines for sequencing data
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machinaFramework for Metastatic And Clonal History INtegrative Analysis
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HMMRATACHMMRATAC peak caller for ATAC-seq data
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ATACseqAnalysis Workflow for Assay for Transposase-Accessible Chromatin using sequencing (ATAC-Seq)
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indigoIndigo: SNV and InDel Discovery in Chromatogram traces obtained from Sanger sequencing of PCR products
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mlst checkMultilocus sequence typing by blast using the schemes from PubMLST
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HtsjdkA Java API for high-throughput sequencing data (HTS) formats.
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catchA package for designing compact and comprehensive capture probe sets.
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OttoSampler, Sequencer, Multi-engine synth and effects - in a box! [WIP]
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gargammelgargammel is an ancient DNA simulator
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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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astarixAStarix: Fast and Optimal Sequence-to-Graph Aligner
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SnapatacAnalysis Pipeline for Single Cell ATAC-seq
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assembly improvementImprove the quality of a denovo assembly by scaffolding and gap filling
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Rnaseq WorkflowA repository for setting up a RNAseq workflow
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pblatparallelized blat with multi-threads support
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HgvsPython library to parse, format, validate, normalize, and map sequence variants. `pip install hgvs`
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SpringFASTQ compression
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CirclatorA tool to circularize genome assemblies
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ga-openai-gymUsage of genetic algorithms to train a neural network in multiple OpenAI gym environments.
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GenomicsA collection of scripts and notes related to genomics and bioinformatics
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gubbinsRapid phylogenetic analysis of large samples of recombinant bacterial whole genome sequences using Gubbins
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GenomicsqliteGenomics Extension for SQLite
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InSilicoSeq🚀 A sequencing simulator
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TruvariStructural variant toolkit for VCFs
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helisaScala API for jenetics
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Mirdeep2Discovering known and novel miRNAs from small RNA sequencing data
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covid-19-signalFiles and methodology pertaining to the sequencing and analysis of SARS-CoV-2, causative agent of COVID-19.
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plasmidtronAssembling the cause of phenotypes and genotypes from NGS data
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tweegeemeeTwitter Genetic Algorithm Imagery
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FluentDNAFluentDNA allows you to browse sequence data of any size using a zooming visualization similar to Google Maps. You can use FluentDNA as a standalone program or as a python module for your own bioinformatics projects.
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scCATCHAutomatic Annotation on Cell Types of Clusters from Single-Cell RNA Sequencing Data
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tracyBasecalling, alignment, assembly and deconvolution of Sanger Chromatogram trace files
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