Explore Workflows
View already parsed workflows here or click here to add your own
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htseq_count_workflow.cwl
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![]() Path: workflows/htseq_count_workflow.cwl Branch/Commit ID: master |
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Align reference proteins plane complete workflow, with miniprot
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![]() Path: protein_alignment/wf_protein_alignment_miniprot.cwl Branch/Commit ID: test |
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strelka workflow
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![]() Path: definitions/subworkflows/strelka_and_post_processing.cwl Branch/Commit ID: master |
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echo.scattered.cwl
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![]() Path: tests/data/echo.scattered.cwl Branch/Commit ID: master |
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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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Whole Exome Sequencing
Whole Exome Sequence analysis using GATK best practices - Germline SNP & Indel Discovery |
![]() Path: packed/exomeseq.cwl Branch/Commit ID: qiime2-workflow Packed ID: main |
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Subworkflow to allow calling different SV callers which require bam files as inputs
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![]() Path: definitions/subworkflows/single_sample_sv_callers.cwl Branch/Commit ID: No_filters_detect_variants |
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wgetkegg_ids.cwl
get KGML by multiple ids |
![]() Path: wgetkegg_ids.cwl Branch/Commit ID: master |
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count-lines9-wf-noET.cwl
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![]() Path: tests/count-lines9-wf-noET.cwl Branch/Commit ID: 1f3ef888d9ef2306c828065c460c1800604f0de4 |
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wf_trim_partial_and_map_se.cwl
This workflow takes in appropriate trimming params and demultiplexed reads, and performs the following steps in order: trimx1, trimx2, fastq-sort, filter repeat elements, fastq-sort, genomic mapping, sort alignment, index alignment, namesort, PCR dedup, sort alignment, index alignment |
![]() Path: cwl/wf_trim_partial_and_map_se.cwl Branch/Commit ID: master |