Explore Workflows
View already parsed workflows here or click here to add your own
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get_spike_in_counts.cwl
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Path: CWL/workflow_modules/get_spike_in_counts.cwl Branch/Commit ID: master |
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sec-wf-out.cwl
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Path: tests/wf/sec-wf-out.cwl Branch/Commit ID: e6a1e1f3a3b3168028bd19aaf465826fa276a35b |
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Find reads with predicted coding sequences above 60 AA in length
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Path: workflows/orf_prediction.cwl Branch/Commit ID: master |
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scatter-wf1.cwl
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Path: tests/scatter-wf1.cwl Branch/Commit ID: main |
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cmsearch-multimodel.cwl
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Path: workflows/cmsearch-multimodel.cwl Branch/Commit ID: 135976d |
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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 |
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collate_unique_SSU_headers.cwl
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Path: tools/collate_unique_SSU_headers.cwl Branch/Commit ID: 0cd2d70 |
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wf_paleocar_web-app_data_flow.cwl
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Path: yw_cwl_modeling/yw_cwl_parser_old/Examples/main/wf_paleocar_web-app_data_flow.cwl Branch/Commit ID: master |
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antibody_campaign.cwl
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Path: workflows/antibody_campaign.cwl Branch/Commit ID: main |
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RNASelector as a CWL workflow
https://doi.org/10.1007/s12275-011-1213-z |
Path: workflows/rna-selector.cwl Branch/Commit ID: ca6ca61 |
