Explore Workflows
View already parsed workflows here or click here to add your own
Graph | Name | Retrieved From | View |
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chksum_xam_to_interleaved_fq.cwl
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![]() Path: cwls/chksum_xam_to_interleaved_fq.cwl Branch/Commit ID: 0.3.2 |
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LSU-from-tablehits.cwl
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![]() Path: tools/LSU-from-tablehits.cwl Branch/Commit ID: master |
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rRNA_selection.cwl
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![]() Path: tools/rRNA_selection.cwl Branch/Commit ID: 708fd97 |
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run_test.cwl
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![]() Path: specfem3d/specfem3d_test_input_cwl/run_test.cwl Branch/Commit ID: master |
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collate_unique_SSU_headers.cwl
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![]() Path: tools/collate_unique_SSU_headers.cwl Branch/Commit ID: c1f8b22 |
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bwameth_singlelib.cwl
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![]() Path: workflows/bwameth/bwameth_singlelib.cwl Branch/Commit ID: main |
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basic.cwl
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![]() Path: cl-tools/workflow/basic.cwl Branch/Commit ID: master |
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Vcf concordance evaluation workflow
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![]() Path: definitions/subworkflows/vcf_eval_concordance.cwl Branch/Commit ID: low-vaf |
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rest_parallel.cwl
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![]() Path: CWL_Workflow/rest_parallel.cwl Branch/Commit ID: main |
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gatk4W-spark.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-spark.cwl Branch/Commit ID: release |