Explore Workflows
View already parsed workflows here or click here to add your own
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04-quantification-se-unstranded.cwl
RNA-seq 04 quantification |
Path: v1.0/RNA-seq_pipeline/04-quantification-se-unstranded.cwl Branch/Commit ID: master |
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step3: create STAR index
create STAR index for mapping CAGE-Seq data (step 1: decompress reference genome fasta file, step 2: create STAR index) |
Path: workflow/02_star_index_subworkflow.cwl Branch/Commit ID: main |
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wf.cwl#main
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Path: wf.cwl Branch/Commit ID: master Packed ID: main |
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gp_makeblastdb
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Path: progs/gp_makeblastdb.cwl Branch/Commit ID: test |
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schemadef-wf.cwl
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Path: tests/schemadef-wf.cwl Branch/Commit ID: master |
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count-lines7-wf.cwl
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Path: v1.0/v1.0/count-lines7-wf.cwl Branch/Commit ID: master |
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module-1
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Path: setup/cwl/module-1.cwl Branch/Commit ID: dev |
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bam-bedgraph-bigwig.cwl
Workflow converts input BAM file into bigWig and bedGraph files. Input BAM file should be sorted by coordinates (required by `bam_to_bedgraph` step). If `split` input is not provided use true by default. Default logic is implemented in `valueFrom` field of `split` input inside `bam_to_bedgraph` step to avoid possible bug in cwltool with setting default values for workflow inputs. `scale` has higher priority over the `mapped_reads_number`. The last one is used to calculate `-scale` parameter for `bedtools genomecov` (step `bam_to_bedgraph`) only in a case when input `scale` is not provided. All logic is implemented inside `bedtools-genomecov.cwl`. `bigwig_filename` defines the output name only for generated bigWig file. `bedgraph_filename` defines the output name for generated bedGraph file and can influence on generated bigWig filename in case when `bigwig_filename` is not provided. All workflow inputs and outputs don't have `format` field to avoid format incompatibility errors when workflow is used as subworkflow. |
Path: tools/bam-bedgraph-bigwig.cwl Branch/Commit ID: master |
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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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timelimit2-wf.cwl
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Path: tests/timelimit2-wf.cwl Branch/Commit ID: master |
