Explore Workflows
View already parsed workflows here or click here to add your own
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wf-variantcall.cwl
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Path: somatic-lowfreq/pisces-ras-workflow/wf-variantcall.cwl Branch/Commit ID: master |
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Averages and aligns the unampped instances
First computes average per UniProt domain instance and then aligns all the average structures against core average structure. Outputs the alignment results along with the structures passing and failing the threshold for given Kpax score. |
Path: Tools/unmapped_unp_avg_align.cwl Branch/Commit ID: main |
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tnsnv-distr.cwl
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Path: stage/tnsnv-distr.cwl Branch/Commit ID: master |
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Subsample BAM file creating a tagAlign and pseudoreplicates
This workflow creates a subsample from a BAM file creating a tagAlign and pseudoreplicates |
Path: workflows/File-formats/subample-pseudoreplicates.cwl Branch/Commit ID: master |
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01-qc-se.cwl
ATAC-seq 01 QC - reads: SE |
Path: v1.0/ATAC-seq_pipeline/01-qc-se.cwl Branch/Commit ID: v1.0.0 |
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03-map-se-blacklist-removal.cwl
ATAC-seq 03 mapping - reads: SE |
Path: v1.0/ATAC-seq_pipeline/03-map-se-blacklist-removal.cwl Branch/Commit ID: v1.0.0 |
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Transcripts annotation workflow
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Path: workflows/TranscriptsAnnotation-i5only-wf.cwl Branch/Commit ID: avoid-spaces |
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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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Unaligned BAM to BQSR and VCF
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Path: definitions/subworkflows/bam_to_bqsr_no_dup_marking.cwl Branch/Commit ID: No_filters_detect_variants |
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Water bodies detection based on NDWI and the otsu threshold
Water bodies detection based on NDWI and otsu threshold applied to a single Sentinel-2 COG STAC item |
Path: cwl-workflow/app-water-body-cloud-native.cwl Branch/Commit ID: main Packed ID: main |
