Explore Workflows
View already parsed workflows here or click here to add your own
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module-4.cwl
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![]() Path: workflows/module-4.cwl Branch/Commit ID: master |
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ST520103.cwl
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![]() Path: wf5201/ST520103.cwl Branch/Commit ID: main |
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Running cellranger count and lineage inference
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![]() Path: definitions/subworkflows/single_cell_rnaseq.cwl Branch/Commit ID: low-vaf |
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ValidateOpticalPSF
Validate telescope (whole dish) optical point-spread function |
![]() Path: workflows/ValidateOpticalPSF.cwl Branch/Commit ID: main |
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exome alignment and germline variant detection
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![]() Path: definitions/pipelines/germline_exome.cwl Branch/Commit ID: downsample_and_recall |
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Production Configuration
This workflow prepares the configuration of the subsequent production steps. |
![]() Path: workflows/wms/uc-wms-XXX.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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BD Rhapsody™ WTA Analysis Pipeline
The BD Rhapsody™ WTA Analysis Pipeline is used to create sequencing libraries from single cell transcriptomes without having to specify a targeted panel. After sequencing, the analysis pipeline takes the FASTQ files, a reference genome file and a transcriptome annotation file for gene alignment. The pipeline generates molecular counts per cell, read counts per cell, metrics, and an alignment file. |
![]() Path: workflow1_11.cwl Branch/Commit ID: main Packed ID: main |
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rp2-to-rp2path.cwl
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![]() Path: workflows/rp2-to-rp2path.cwl Branch/Commit ID: master |
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preprocess_vcf.cwl
This workflow will perform preprocessing steps on VCFs for the OxoG/Variantbam/Annotation workflow. |
![]() Path: preprocess_vcf.cwl Branch/Commit ID: 1.0.0 |