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picard_markduplicates
Mark duplicates |
![]() Path: structuralvariants/cwl/abstract_operations/subworkflows/picard_markduplicates.cwl Branch/Commit ID: de9cb009f8fe0c8d5a94db5c882cf21ddf372452 |
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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: f2dab2d4e626a2a840fa840d7b190a82d4200b21 |
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THOR - differential peak calling of ChIP-seq signals with replicates
What is THOR? -------------- THOR is an HMM-based approach to detect and analyze differential peaks in two sets of ChIP-seq data from distinct biological conditions with replicates. THOR performs genomic signal processing, peak calling and p-value calculation in an integrated framework. For more information please refer to: ------------------------------------- Allhoff, M., Sere K., Freitas, J., Zenke, M., Costa, I.G. (2016), Differential Peak Calling of ChIP-seq Signals with Replicates with THOR, Nucleic Acids Research, epub gkw680. |
![]() Path: workflows/rgt-thor.cwl Branch/Commit ID: b4d578c2ba4713a5a22163d9f8c7105acda1f22e |
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scatter-valuefrom-wf6.cwl
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![]() Path: cwltool/schemas/v1.0/v1.0/scatter-valuefrom-wf6.cwl Branch/Commit ID: e4a52682f3bdefafe5c27e32983fed31116ac489 |
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816_wf.cwl
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![]() Path: tests/wf/816_wf.cwl Branch/Commit ID: d3c7bd5d6c409e857b98f9034a55952ca95afdb3 |
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umi molecular alignment workflow
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![]() Path: definitions/subworkflows/molecular_qc.cwl Branch/Commit ID: ad65dc1dfff9afa5077f498b85e699716c47f6cb |
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scatter-wf2_v1_1.cwl
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![]() Path: testdata/scatter-wf2_v1_1.cwl Branch/Commit ID: 124a08ce3389eb49066c34a4163cbbed210a0355 |
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exome alignment and germline variant detection
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![]() Path: definitions/subworkflows/germline_detect_variants.cwl Branch/Commit ID: e7e888df9e7d44f036c4c7985e474016ee9e6525 |
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Varscan Workflow
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![]() Path: definitions/subworkflows/varscan_germline.cwl Branch/Commit ID: e59c77629936fad069007ba642cad49fef7ad29f |
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alignment_novoalign.cwl
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![]() Path: genomel/cwl/workflows/harmonization/alignment_novoalign.cwl Branch/Commit ID: 7f01768479e6a77a5caf6b3382174aa038ba05fc |