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Showing results for "rnaseq" (Show all)
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rnaseq-header.cwl
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Path: metadata/rnaseq-header.cwl Branch/Commit ID: b141f7e73005227d6d02fa03a47151836dd4109b |
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xenbase-rnaseq-pe.cwl
XenBase workflow for analysing RNA-Seq paired-end data |
Path: workflows/xenbase-rnaseq-pe.cwl Branch/Commit ID: 6e09b4bf1ff0eb3dd1294f5578624c5a2a2b0b37 |
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rnaseq-header.cwl
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Path: metadata/rnaseq-header.cwl Branch/Commit ID: d47fdb25c56124dadd33b05a90273f64064d69e4 |
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rnaseq-header.cwl
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Path: metadata/rnaseq-header.cwl Branch/Commit ID: 12c29f88855329192bfff977f046990031f04931 |
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rnaseq_pipeline_fastq_checker-tar.cwl
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Path: workflow/checker-workflows/rnaseq_pipeline_fastq_checker-tar.cwl Branch/Commit ID: 06c6ff20f4e719d7f7224c17b22dce8617e92447 |
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rnaseq-header.cwl
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Path: metadata/rnaseq-header.cwl Branch/Commit ID: 948bc3e211ce14bcdaf4f026d3695d16f423ca4a |
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rnaseq-header.cwl
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Path: metadata/rnaseq-header.cwl Branch/Commit ID: 3ceeb2e90f49579369b2e10485908516348381a9 |
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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: b465f0da2806ddb6df481409541d13288ccb40ec |
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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: fcab170f3e8a4bc70601650401cce2a9df42f484 |
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rnaseq-header.cwl
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Path: metadata/rnaseq-header.cwl Branch/Commit ID: 0ddfca10c41f83bb120c7633e0db9dba7441bca0 |
