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Showing results for "rnaseq" (Show all)
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rnaseq-se.cwl
RNA-Seq basic analysis workflow for single-read experiment. |
Path: workflows/rnaseq-se.cwl Branch/Commit ID: cf107bc24a37883ef01b959fd89c19456aaecc02 |
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rnaseq_metrics_workflow.cwl
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Path: rnaseq-star-align/subworkflows/rnaseq_processing/rnaseq_metrics_workflow.cwl Branch/Commit ID: 88fb720c62a3c2b00ca475d412fba088c4a08f92 |
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rnaseq-header.cwl
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Path: metadata/rnaseq-header.cwl Branch/Commit ID: e119c5908d0a1f2ef1765fd612107cfc3494b8b6 |
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Workflow to run pVACseq from detect_variants and rnaseq pipeline outputs
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Path: definitions/subworkflows/pvacseq.cwl Branch/Commit ID: c23dc7f113ca0b0a3127a5d6c696e98d4799460c |
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rnaseq-se.cwl
RNA-Seq basic analysis workflow for single-read experiment. |
Path: workflows/rnaseq-se.cwl Branch/Commit ID: 3ceeb2e90f49579369b2e10485908516348381a9 |
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samtoolsW.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: samtoolsW.cwl Branch/Commit ID: f2dab2d4e626a2a840fa840d7b190a82d4200b21 |
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xenbase-rnaseq-se.cwl
XenBase workflow for analysing RNA-Seq single-end data |
Path: workflows/xenbase-rnaseq-se.cwl Branch/Commit ID: 2d00e7f29c72d33b70dcd46b58db1fc31a7f2d86 |
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Workflow to run pVACseq from detect_variants and rnaseq pipeline outputs
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Path: definitions/subworkflows/pvacseq.cwl Branch/Commit ID: 0805e8e0d358136468e0a9f49e06005e41965adc |
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allele-rnaseq-se.cwl
Allele specific RNA-Seq single-read workflow |
Path: workflows/allele-rnaseq-se.cwl Branch/Commit ID: 94471ee6c01b7bc17102e45e56e7366c2a52acdf |
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rnaseq-pe.cwl
RNA-Seq basic analysis workflow for paired-end experiment. |
Path: workflows/rnaseq-pe.cwl Branch/Commit ID: 62323c137c0ce9b3f843df0dfbda28dafa7c90cf |
