Explore Workflows
View already parsed workflows here or click here to add your own
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find_hotspots_in_normals.cwl
Workflow to find hotspot VAFs from duplex (for Tumor sample) and unfiltered (for Normal sample) pileups. These inputs are all required to be sorted in the same order: sample_ids patient_ids sample_classes unfiltered_pileups duplex_pileups |
![]() Path: workflows/subworkflows/find_hotspots_in_normals.cwl Branch/Commit ID: master |
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Apply filters to VCF file
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![]() Path: definitions/subworkflows/filter_vcf.cwl Branch/Commit ID: master |
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Low vaf Detect Variants workflow for Megan Cooper
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![]() Path: definitions/pipelines/low_vaf_detect_variants.cwl Branch/Commit ID: low-vaf |
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wf-loadContents.cwl
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![]() Path: tests/wf-loadContents.cwl Branch/Commit ID: main |
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Sentinel-3 SLSTR Level-2 reprojection and tiling
This service takes as input a Sentinel-3 SLSTR Level 2 (SL_2_LST____) product on DESCENDING pass and does the reprojection and tiling |
![]() Path: docs/examples/slstr-tiling.cwl Branch/Commit ID: master Packed ID: slstr-tiling |
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Functional analyis of sequences that match the 16S SSU
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![]() Path: workflows/16S_taxonomic_analysis.cwl Branch/Commit ID: 5dc7c5c |
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main.cwl
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![]() Path: main.cwl Branch/Commit ID: master |
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varscanW.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: varscanW.cwl Branch/Commit ID: release |
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rhapsody_targeted_1.9-beta.cwl#UncompressDatatables.cwl
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![]() Path: v1.9-beta/rhapsody_targeted_1.9-beta.cwl Branch/Commit ID: master Packed ID: UncompressDatatables.cwl |
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minibam_sub_wf.cwl
This is a subworkflow of the main oxog_varbam_annotat_wf workflow - this is not meant to be run as a stand-alone workflow! |
![]() Path: minibam_sub_wf.cwl Branch/Commit ID: 1.0.0 |