Explore Workflows
View already parsed workflows here or click here to add your own
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Build STAR indices
Workflow runs [STAR](https://github.com/alexdobin/STAR) v2.5.3a (03/17/2017) PMID: [23104886](https://www.ncbi.nlm.nih.gov/pubmed/23104886) to build indices for reference genome provided in a single FASTA file as fasta_file input and GTF annotation file from annotation_gtf_file input. Generated indices are saved in a folder with the name that corresponds to the input genome. |
Path: workflows/star-index.cwl Branch/Commit ID: 91bb63948c0a264334b9007ef85f936768d90d11 |
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exome alignment and germline variant detection
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Path: definitions/subworkflows/germline_detect_variants.cwl Branch/Commit ID: 0c4f4e59c265eb22aed3d2d37b173cb5430773d2 |
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AltAnalyze Build Reference Indices
AltAnalyze Build Reference Indices ================================== |
Path: workflows/altanalyze-prepare-genome.cwl Branch/Commit ID: f3e44d3b0f198cf5245c49011124dc3b6c2b06fd |
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Raw sequence data to BQSR
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Path: definitions/subworkflows/sequence_to_bqsr.cwl Branch/Commit ID: 60edaf6f57eaaf02cda1a3d8cb9a825aa64a43e2 |
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io-int-wf.cwl
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Path: tests/io-int-wf.cwl Branch/Commit ID: 31ec48a8d81ef7c1b2c5e9c0a19e7623efe4a1e2 |
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pcr-bottleneck-coef.cwl
ChIP-seq - map - PCR Bottleneck Coefficients |
Path: v1.0/map/pcr-bottleneck-coef.cwl Branch/Commit ID: f053d1a92762b38b950c4982e3b344cec26f4f36 |
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merge and annotate svs with population allele freq and vep
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Path: definitions/subworkflows/merge_svs.cwl Branch/Commit ID: a9133c999502acf94b433af8d39897e6c2cdf65f |
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Subworkflow that runs cnvkit in single sample mode and returns a vcf file
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Path: definitions/subworkflows/cnvkit_single_sample.cwl Branch/Commit ID: a9133c999502acf94b433af8d39897e6c2cdf65f |
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SV filtering workflow
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Path: definitions/subworkflows/filter_sv_vcf.cwl Branch/Commit ID: a9133c999502acf94b433af8d39897e6c2cdf65f |
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psortedDefaultParams.cwl
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Path: steps/psortedDefaultParams.cwl Branch/Commit ID: 5b866e480fb557cf53d619a22068c73548e337d5 |
