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GalaxyData intensive science for everyone.
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Brunch🍴 Web applications made easy. Since 2011.
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PipelinePipeline is a package to build multi-staged concurrent workflows with a centralized logging output.
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ToilA scalable, efficient, cross-platform (Linux/macOS) and easy-to-use workflow engine in pure Python.
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BatchflowBatchFlow helps you conveniently work with random or sequential batches of your data and define data processing and machine learning workflows even for datasets that do not fit into memory.
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ngs-preprocessA pipeline for preprocessing NGS data from Illumina, Nanopore and PacBio technologies
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Drake ExamplesExample workflows for the drake R package
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AtacseqATAC-seq peak-calling, QC and differential analysis pipeline
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needlestackMulti-sample somatic variant caller
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TargetsFunction-oriented Make-like declarative workflows for R
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PHATPathogen-Host Analysis Tool - A modern Next-Generation Sequencing (NGS) analysis platform
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Jenkins Workflowcontains handy groovy workflow-libs scripts
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rvtestsRare variant test software for next generation sequencing data
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IARC-nfList of IARC bioinformatics nextflow pipelines
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MTBseq sourceMTBseq is an automated pipeline for mapping, variant calling and detection of resistance mediating and phylogenetic variants from illumina whole genome sequence data of Mycobacterium tuberculosis complex isolates.
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simpleflowPython library for dataflow programming.
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gencoreGenerate duplex/single consensus reads to reduce sequencing noises and remove duplications
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nactivityworkflow engine activity activiti
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germline-DNAA BioWDL variantcalling pipeline for germline DNA data. Starting with FASTQ files to produce VCF files. Category:Multi-Sample
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plasmidtronAssembling the cause of phenotypes and genotypes from NGS data
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dropEstPipeline for initial analysis of droplet-based single-cell RNA-seq data
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