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samtoolsW.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 VARSCAN. It is hoped to be effective and useful for getting SARS-CoV-2 genome variants. It uses Illumina RNASEQ reads and genome sequence. |
![]() Path: samtoolsW.cwl Branch/Commit ID: 690ff2fa1ef356c42003e4b9986d39f4e44806a8 |
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mutect panel-of-normals workflow
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![]() Path: definitions/pipelines/panel_of_normals.cwl Branch/Commit ID: d3e4bf55753cd92f97537c7d701187ea92d1e5f0 |
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count-lines7-wf_v1_2.cwl
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![]() Path: testdata/count-lines7-wf_v1_2.cwl Branch/Commit ID: 124a08ce3389eb49066c34a4163cbbed210a0355 |
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mutect panel-of-normals workflow
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![]() Path: definitions/pipelines/panel_of_normals.cwl Branch/Commit ID: 735be84cdea041fcc8bd8cbe5728b29ca3586a21 |
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word-mapping-test-files-wf.cwl#align-texts-wf.cwl
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![]() Path: ochre/cwl/word-mapping-test-files-wf.cwl Branch/Commit ID: a62bf3b31df83784c017d30a83ed8e01d454bf1c Packed ID: align-texts-wf.cwl |
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count-lines7-single-source-wf_v1_2.cwl
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![]() Path: testdata/count-lines7-single-source-wf_v1_2.cwl Branch/Commit ID: 0ad6983898f0d9001fe0f416f97c4d8b940e384a |
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readgroup_fastq_se.cwl
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![]() Path: workflows/bamfastq_align/readgroup_fastq_se.cwl Branch/Commit ID: 6b43e8b03256492f2b36ffcf548704daaafee6f6 |
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scatter-valuefrom-wf6.cwl
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![]() Path: tests/scatter-valuefrom-wf6.cwl Branch/Commit ID: e62f99dd79d6cb9c157cceb458f74200da84f6e9 |
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WGS QC workflow mouse
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![]() Path: definitions/subworkflows/qc_wgs_mouse.cwl Branch/Commit ID: 3042812447d9e8889c6118986490e9c9b9b13223 |
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scatter-wf3.cwl#main
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![]() Path: tests/scatter-wf3.cwl Branch/Commit ID: 57baec040c99d7edef8242ef51b5470b1c82d733 Packed ID: main |