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Showing results for "rnaseq" (Show all)
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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: a9133c999502acf94b433af8d39897e6c2cdf65f |
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rnaseq-pe-dutp-mitochondrial.cwl
RNA-Seq strand specific mitochondrial workflow for pair-end experiment based on BioWardrobe's basic analysis. |
Path: workflows/rnaseq-pe-dutp-mitochondrial.cwl Branch/Commit ID: cf107bc24a37883ef01b959fd89c19456aaecc02 |
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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: 18600518ce6539a2e29c1707392a4c5da5687fa3 |
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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: 2e0562a5c3cd7aac24af4c622a5ae68a7fb23a71 |
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rnaseq-alignment-quantification
This workflow retrieve SRA fastqc data and execute QC, alignment and quantification from TPMCalculator |
Path: workflows/RNA-Seq/rnaseq-alignment-quantification.cwl Branch/Commit ID: e541470bc9d0b064bc4ed7dd2b45d8ec67760613 |
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trim-rnaseq-se.cwl
Runs RNA-Seq BioWardrobe basic analysis with single-end data file. |
Path: workflows/trim-rnaseq-se.cwl Branch/Commit ID: 801f7b363e0599b9a28ecda696dfdb1c0e40ce71 |
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rnaseq_metrics_workflow.cwl
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Path: workflows/subworkflows/rnaseq_processing/rnaseq_metrics_workflow.cwl Branch/Commit ID: 490ff7f2595262eb883b5804462afaf70e7bc2e1 |
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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: 3034168d652bfa930ba09af20e473a4564a8010d |
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Ambarish_Kumar_SOP-GATK-SAR-CoV-2.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: Ambarish_Kumar_SOP/Ambarish_Kumar_SOP-GATK-SAR-CoV-2.cwl Branch/Commit ID: 2c47ee8b02219cf9959f7ad5e4cf2e6d6f5b0601 |
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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: 530e671c113e91fe6b9114eda32103bb980450c7 |
