Explore Workflows
View already parsed workflows here or click here to add your own
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rRNA_selection.cwl
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Path: tools/rRNA_selection.cwl Branch/Commit ID: 0fed1c9 |
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blast.cwl
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Path: wdl2cwl/tests/cwl_files/blast.cwl Branch/Commit ID: main |
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ndppp-pipeline.cwl
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Path: ndppp-pipeline.cwl Branch/Commit ID: master |
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collate_unique_SSU_headers.cwl
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Path: tools/collate_unique_SSU_headers.cwl Branch/Commit ID: f993cad |
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bams2gvcf.woBQSR_male_chrXY_wXTR.cwl
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Path: Workflows/bams2gvcf.woBQSR_male_chrXY_wXTR.cwl Branch/Commit ID: master |
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bams2gvcf.wBQSR.cwl
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Path: Workflows/bams2gvcf.wBQSR.cwl Branch/Commit ID: master |
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Per-chromosome pindel
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Path: definitions/subworkflows/pindel_cat.cwl Branch/Commit ID: No_filters_detect_variants |
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biowardrobe_chipseq_se.cwl
The workflow is used to run CHIP-Seq basic analysis with single-end input FASTQ file. In outputs it returns coordinate sorted BAM file alongside with index BAI file, quality statistics of the input FASTQ file, reads coverage in a form of bigWig file, peaks calling data in a form of narrowPeak or broadPeak files. |
Path: biowardrobe_chipseq_se.cwl Branch/Commit ID: master |
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map medium and long reads (greater than 100 bp) against reference genome
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Path: bwa/BWA-Mem2-paired.cwl Branch/Commit ID: release |
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qiime2 explore sample taxonomic composition
Taxonomic analysis from https://docs.qiime2.org/2018.4/tutorials/moving-pictures/ |
Path: packed/qiime2-step2-dada2-paired.cwl Branch/Commit ID: qiime2-workflow-paired Packed ID: qiime2-08-taxonomic-analysis.cwl |
