Explore Workflows
View already parsed workflows here or click here to add your own
Graph | Name | Retrieved From | View |
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Filter single sample sv vcf from depth callers(cnvkit/cnvnator)
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![]() Path: definitions/subworkflows/sv_depth_caller_filter.cwl Branch/Commit ID: 9e5f228bc1a3d0dfe950b5d41d7e4319e834a6d4 |
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topmed-alignment.cwl
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![]() Path: aligner/sbg-alignment-cwl/topmed-alignment.cwl Branch/Commit ID: de683e0be7c2798b3eb503812a095659039247b3 |
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Merge, annotate, and generate a TSV for SVs
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![]() Path: definitions/subworkflows/merge_svs.cwl Branch/Commit ID: 9e5f228bc1a3d0dfe950b5d41d7e4319e834a6d4 |
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scRNA-seq pipeline using Salmon and Alevin
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![]() Path: pipeline.cwl Branch/Commit ID: 4db77ce1de9019ac997dd5da553ea0f11a15d9f9 |
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topmed-alignment.cwl
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![]() Path: aligner/sbg-alignment-cwl/topmed-alignment.cwl Branch/Commit ID: 6478d5df50d7340311d18f03a056e3db97811269 |
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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: 530e671c113e91fe6b9114eda32103bb980450c7 |
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process VCF workflow
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![]() Path: definitions/subworkflows/strelka_process_vcf.cwl Branch/Commit ID: 87faba2fff8007ecc95160729b1c7cd0376e46f2 |
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filter-pcr-artifacts.cwl
DNase-seq - map - Filter PCR Artifacts |
![]() Path: v1.0/map/filter-pcr-artifacts.cwl Branch/Commit ID: 4e568335133405d28f4b73ae11e7f51f2900dfa3 |
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WGS QC workflow mouse
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![]() Path: definitions/subworkflows/qc_wgs_mouse.cwl Branch/Commit ID: bed420556091b7b8b45cf20a95e5947e1de9a416 |
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Hello World
Outputs a message using echo |
![]() Path: workflows/workflows/hello/hello-param.cwl Branch/Commit ID: 4e568335133405d28f4b73ae11e7f51f2900dfa3 |