Explore Workflows
View already parsed workflows here or click here to add your own
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schemadef-wf.cwl
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![]() Path: cwltool/schemas/v1.0/v1.0/schemadef-wf.cwl Branch/Commit ID: 819c81af5449ec912bbbbead042ad66b8d3fd8d4 |
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pipeline.cwl
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![]() Path: tools/pipeline.cwl Branch/Commit ID: dd2f03cc8a0ca7bc644968ac0c34d4502d6da093 |
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kf_jointgenotyping_workflow_optimized.cwl
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![]() Path: workflow/kf_jointgenotyping_workflow_optimized.cwl Branch/Commit ID: 9c5671e49e5e47cbe872c7b873c5e479c6aaf973 |
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grep-and-count.cwl
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![]() Path: grep-and-count.cwl Branch/Commit ID: bff3770d52404b12d2d0f12b45c4c0edd3213dba |
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Filter Protein Seeds; Find ProSplign Alignments
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![]() Path: protein_alignment/wf_compart_filter_prosplign.cwl Branch/Commit ID: 7c8eb4d23c3c9859f57421643710c0b6d57b606c |
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gatk4W.cwl
Author: AMBARISH KUMAR er.ambarish@gmail.com & ambari73_sit@jnu.ac.in This is a proposed standard operating procedure for genomic variant detection using GATK4. It is hoped to be effective and useful for getting SARS-CoV-2 genome variants. It uses Illumina RNASEQ reads and genome sequence. |
![]() Path: gatk4W.cwl Branch/Commit ID: 530e671c113e91fe6b9114eda32103bb980450c7 |
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coverage.cwl
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![]() Path: tools/stats/coverage.cwl Branch/Commit ID: dd2f03cc8a0ca7bc644968ac0c34d4502d6da093 |
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Bacterial Annotation, pass 1, genemark training, by HMMs (first pass)
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![]() Path: bacterial_annot/wf_bacterial_annot_pass1.cwl Branch/Commit ID: 7c8eb4d23c3c9859f57421643710c0b6d57b606c |
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workflow.cwl
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![]() Path: flow_dispatch/2other_species/workflow.cwl Branch/Commit ID: 45bb8fc5cc5e5fee3f29099469621a53d084757d |
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downsample unaligned BAM and align
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![]() Path: definitions/subworkflows/downsampled_alignment.cwl Branch/Commit ID: 67f56d3b9c70ad56019ed8aa8d50a128e02be43b |