Explore Workflows
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wf_trim_and_map_chimeric_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_and_map_chimeric_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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count-lines18-wf.cwl
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![]() Path: tests/count-lines18-wf.cwl Branch/Commit ID: main |
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03-map-pe.cwl
STARR-seq 03 mapping - reads: PE |
![]() Path: v1.0/STARR-seq_pipeline/03-map-pe.cwl Branch/Commit ID: master |
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count-lines11-null-step-wf-noET.cwl
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![]() Path: tests/count-lines11-null-step-wf-noET.cwl Branch/Commit ID: main |
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wf_makeblastdb.cwl
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![]() Path: amr_finder/wf_makeblastdb.cwl Branch/Commit ID: master |
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gvcf-distr.cwl
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![]() Path: stage/gvcf-distr.cwl Branch/Commit ID: master |
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gatk4W-spark.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: gatk4W-spark.cwl Branch/Commit ID: release |
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dna.cwl#main
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![]() Path: workflows/make-to-cwl/dna.cwl Branch/Commit ID: master Packed ID: main |
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collate_unique_SSU_headers.cwl
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![]() Path: tools/collate_unique_SSU_headers.cwl Branch/Commit ID: a8abd0e |