Explore Workflows
View already parsed workflows here or click here to add your own
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Add snv and indel bam-readcount files to a vcf
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Path: definitions/subworkflows/vcf_readcount_annotator.cwl Branch/Commit ID: 038cb3617a1966a1057386adcde97ce55d9e1139 |
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bam_readcount workflow
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Path: definitions/subworkflows/bam_readcount.cwl Branch/Commit ID: eb0092603bf57acb7bda08a06e4f2f1e2a8c9b6d |
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count-lines11-wf.cwl
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Path: v1.0/v1.0/count-lines11-wf.cwl Branch/Commit ID: fe164457f370c2dfec5156f6d6d45818d53cb871 |
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scatter GATK HaplotypeCaller over intervals
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Path: definitions/subworkflows/gatk_haplotypecaller_iterator.cwl Branch/Commit ID: 54846feabbf008c1946db2a86d87252e0edd95b0 |
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protein_extract
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Path: progs/protein_extract.cwl Branch/Commit ID: dcbbce152fbff2637f102471fb80318244492853 |
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1st-workflow.cwl
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Path: cwltool/schemas/v1.0/examples/1st-workflow.cwl Branch/Commit ID: e6c2d955a448225f026a04130443d13661844440 |
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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: dccb12c85526c878ce3a489f9502350d187955a5 |
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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: 25129f55226dee595ef941edc24d3c44414e0523 |
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Apply filters to VCF file
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Path: definitions/subworkflows/germline_filter_vcf.cwl Branch/Commit ID: 54846feabbf008c1946db2a86d87252e0edd95b0 |
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assm_assm_blastn_wnode
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Path: task_types/tt_assm_assm_blastn_wnode.cwl Branch/Commit ID: f225cd99b0e0a5043dd102f8b33a6139fefe9ea4 |
