Explore Workflows
View already parsed workflows here or click here to add your own
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beagle-imputation-scatter-region.cwl
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Path: Workflows/beagle-imputation-scatter-region.cwl Branch/Commit ID: main |
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wf_clipseqcore_nostats_se_1barcode.cwl
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Path: cwl/wf_clipseqcore_nostats_se_1barcode.cwl Branch/Commit ID: master |
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QIIME2 Step 2 (Deblur option)
QIIME2 Deblur, feature summaries, phylogenetic diversity tree, taxonomic analysis and ancom |
Path: packed/qiime2-step2-deblur.cwl Branch/Commit ID: qiime2-workflow-paired Packed ID: main |
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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: release |
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pangenome-generate_spoa.cwl
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Path: pangenome-generate_spoa.cwl Branch/Commit ID: main |
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count-lines11-wf.cwl
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Path: v1.0/v1.0/count-lines11-wf.cwl Branch/Commit ID: master |
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gathered exome alignment and somatic variant detection for cle purpose
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Path: definitions/pipelines/somatic_exome_cle_gathered.cwl Branch/Commit ID: low-vaf |
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LSU-from-tablehits.cwl
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Path: tools/LSU-from-tablehits.cwl Branch/Commit ID: f914942 |
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snaptools_create_snap_file.cwl
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Path: snaptools_create_snap_file.cwl Branch/Commit ID: feature/docker_cwl |
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WGSSomaticMultiCallers_1_4_0.cwl
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Path: janis_pipelines/wgs_somatic/cwl/WGSSomaticMultiCallers_1_4_0.cwl Branch/Commit ID: master |
