Explore Workflows
View already parsed workflows here or click here to add your own
Graph | Name | Retrieved From | View |
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Kallisto index pipeline
This workflow indexes the input reference FASTA with kallisto, and generates a kallisto index file (.kdx). This index sample can then be used as input into the kallisto transcript-level quantification workflow (kallisto-quant-pe.cwl), or others that may include this workflow as an upstream source. ### __Inputs__ - FASTA file of the reference genome that will be indexed - number of threads to use for multithreading processes ### __Outputs__ - kallisto index file (.kdx). - stdout log file (output in Overview tab as well) - stderr log file ### __Data Analysis Steps__ 1. cwl calls dockercontainer robertplayer/scidap-kallisto to index reference FASTA with `kallisto index`, generating a kallisto index file. ### __References__ - Bray, N. L., Pimentel, H., Melsted, P. & Pachter, L. Near-optimal probabilistic RNA-seq quantification, Nature Biotechnology 34, 525-527(2016), doi:10.1038/nbt.3519 |
![]() Path: workflows/kallisto-index.cwl Branch/Commit ID: master |
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04-quantification-se-revstranded.cwl
RNA-seq 04 quantification |
![]() Path: v1.0/RNA-seq_pipeline/04-quantification-se-revstranded.cwl Branch/Commit ID: master |
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dropEst pipeline
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![]() Path: dropest.cwl Branch/Commit ID: master |
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host_process.cwl
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![]() Path: host_process.cwl Branch/Commit ID: main |
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main-NA12878-platinum-chr20.cwl
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![]() Path: NA12878-platinum-chr20-workflow/main-NA12878-platinum-chr20.cwl Branch/Commit ID: master |
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exomeseq-gatk4-03-organizedirectories.cwl
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![]() Path: subworkflows/exomeseq-gatk4-03-organizedirectories.cwl Branch/Commit ID: master |
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qiime2 importing data
Obtaining and importing data from https://docs.qiime2.org/2018.4/tutorials/moving-pictures/ |
![]() Path: packed/qiime2-step1-import-demux-paired.cwl Branch/Commit ID: qiime2-workflow-paired Packed ID: qiime2-01-import-data-paired.cwl |
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somatic_exome: exome alignment and somatic variant detection
somatic_exome is designed to perform processing of mutant/wildtype H.sapiens exome sequencing data. It features BQSR corrected alignments, 4 caller variant detection, and vep style annotations. Structural variants are detected via manta and cnvkit. In addition QC metrics are run, including somalier concordance metrics. example input file = analysis_workflows/example_data/somatic_exome.yaml |
![]() Path: definitions/pipelines/somatic_exome.cwl Branch/Commit ID: master |
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rRNA_selection.cwl
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![]() Path: tools/rRNA_selection.cwl Branch/Commit ID: 930a2cf |
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Trim and reformat reads (single and paired end version)
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![]() Path: workflows/trim_and_reformat_reads.cwl Branch/Commit ID: 71d9c83 |