Explore Workflows
View already parsed workflows here or click here to add your own
Graph | Name | Retrieved From | View |
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alignment workflow
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![]() Path: assets/CWL/workflow.cwl Branch/Commit ID: master |
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kmer_cache_store
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![]() Path: task_types/tt_kmer_cache_store.cwl Branch/Commit ID: dev |
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downsample unaligned BAM and align
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![]() Path: definitions/subworkflows/downsampled_alignment.cwl Branch/Commit ID: No_filters_detect_variants |
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Ambarish_Kumar_SOP-GATK-SAR-CoV-2.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 GATK4. It is hoped to be effective and useful for getting SARS-CoV-2 genome variants. It uses Illumina RNASEQ reads and genome sequence. |
![]() Path: Ambarish_Kumar_SOP/Ambarish_Kumar_SOP-GATK-SAR-CoV-2.cwl Branch/Commit ID: main |
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clipAteam.cwl
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![]() Path: workflows/clipAteam.cwl Branch/Commit ID: master |
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TransDecoder 2 step workflow, running TransDecoder.LongOrfs (step 1) followed by TransDecoder.Predict (step2)
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![]() Path: workflows/TransDecoder-v5-wf-2steps.cwl Branch/Commit ID: avoid-spaces |
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facets.cwl
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![]() Path: modules/pair/facets.cwl Branch/Commit ID: master |
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step2: trimming fastq files (paired-end)
multiple fastq files trimming process using fastp version 0.23.4 and scatter feature requirement |
![]() Path: workflow/01_trimming_fastq_subworkflow_pe.cwl Branch/Commit ID: main |
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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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step4: STAR for CAGE-Seq reads analysis
STAR for CAGE-Seq reads analysis |
![]() Path: workflow/03_star4cageseq_analysis_subworkflow_pe.cwl Branch/Commit ID: main |