Explore Workflows
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Graph | Name | Retrieved From | View |
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scatter-wf2.cwl
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![]() Path: tests/scatter-wf2.cwl Branch/Commit ID: main |
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qiime2 demux sequences
Demultiplexing sequences from https://docs.qiime2.org/2018.4/tutorials/moving-pictures/ |
![]() Path: subworkflows/qiime2-02-demux-emp-single.cwl Branch/Commit ID: develop |
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Single-cell RNA-Seq Aggregate
Single-cell RNA-Seq Aggregate Aggregates gene expression data from multiple Single-cell RNA-Seq Alignment experiments. |
![]() Path: workflows/sc-rna-aggregate-wf.cwl Branch/Commit ID: main |
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Detect Docm variants
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![]() Path: definitions/subworkflows/docm_cle.cwl Branch/Commit ID: master |
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04-quantification-pe-stranded.cwl
RNA-seq 04 quantification |
![]() Path: v1.0/RNA-seq_pipeline/04-quantification-pe-stranded.cwl Branch/Commit ID: master |
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cnv_manta
CNV Manta calling |
![]() Path: structuralvariants/cwl/abstract_operations/subworkflows/cnv_manta.cwl Branch/Commit ID: master |
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ST520112.cwl
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![]() Path: ST520112.cwl Branch/Commit ID: main |
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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: release |
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wgs alignment with qc
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![]() Path: wgs_alignment.cwl Branch/Commit ID: e4c851d65f460e8f48ca184120044fce72cb2433 |
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qiime2 Deblur detect/correct sequence data
Option 2: Deblur from https://docs.qiime2.org/2018.4/tutorials/moving-pictures/ |
![]() Path: subworkflows/qiime2-03-deblur.cwl Branch/Commit ID: develop |