Explore Workflows
View already parsed workflows here or click here to add your own
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bulk scRNA-seq pipeline using Salmon
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Path: bulk-pipeline.cwl Branch/Commit ID: d18fd4992c69eadfad82186d1e16a07092477552 |
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chipseq-pe.cwl
Runs ChIP-Seq BioWardrobe basic analysis with paired-end input data files. |
Path: workflows/chipseq-pe.cwl Branch/Commit ID: 94c6ea7bf4b64599746d778568efbd8e10f0d5ba |
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Bacterial Annotation, ab initio (first pass) searched against AntiFam
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Path: bacterial_annot/wf_ab_initio_antifam.cwl Branch/Commit ID: 6a456869b53513bff31fec02cc5ea3cc26fede36 |
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Run genomic CMsearch (Rfam rRNA)
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Path: bacterial_ncrna/wf_gcmsearch.cwl Branch/Commit ID: 6a456869b53513bff31fec02cc5ea3cc26fede36 |
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Bacterial Annotation, pass 1, genemark training, by HMMs (first pass)
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Path: bacterial_annot/wf_orf_hmms.cwl Branch/Commit ID: 6a456869b53513bff31fec02cc5ea3cc26fede36 |
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Detect Variants workflow
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Path: definitions/pipelines/detect_variants_mouse.cwl Branch/Commit ID: adcae308fdccaa1190083616118dfadb4df65dca |
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umi molecular alignment fastq workflow
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Path: definitions/pipelines/alignment_umi_molecular.cwl Branch/Commit ID: 457e101e3fb87e7fd792357afce00ed8ccbfbcdb |
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PGAP Pipeline, simple user input, PGAPX-134
PGAP pipeline for external usage, powered via containers, simple user input: (FASTA + yaml only, no template) |
Path: pgap.cwl Branch/Commit ID: e2832ecc1c5f64a9e522bb1b24cd45f8bb2ca429 |
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harmonization_novoalign_multi_readgroup.cwl
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Path: genomel/cwl/workflows/harmonization/harmonization_novoalign_multi_readgroup.cwl Branch/Commit ID: d777030ca3654fe78462ee69adcbd8221303b006 |
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search.cwl#main
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Path: cwltool/schemas/v1.0/v1.0/search.cwl Branch/Commit ID: b3639a4c5075abc562b7f9b816be0d4f7d711703 Packed ID: main |
