Explore Workflows
View already parsed workflows here or click here to add your own
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Find reads with predicted coding sequences above 60 AA in length
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![]() Path: workflows/orf_prediction.cwl Branch/Commit ID: master |
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module-3.cwl
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![]() Path: workflows/module-3.cwl Branch/Commit ID: master |
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functional analysis prediction with InterProScan
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![]() Path: workflows/functional_analysis.cwl Branch/Commit ID: master |
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EMG assembly for paired end Illumina
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![]() Path: workflows/emg-assembly.cwl Branch/Commit ID: 0cd2d70 |
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EMG assembly for paired end Illumina
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![]() Path: workflows/emg-assembly.cwl Branch/Commit ID: 5833078 |
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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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word-mapping-test-files-wf.cwl#align-texts-wf.cwl
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![]() Path: ochre/cwl/word-mapping-test-files-wf.cwl Branch/Commit ID: master Packed ID: align-texts-wf.cwl |
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workflow_select_shape.cwl
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![]() Path: cwl/workflow_select_shape.cwl Branch/Commit ID: master |
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fp_filter workflow
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![]() Path: definitions/subworkflows/fp_filter.cwl Branch/Commit ID: low-vaf |
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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 |