Explore Workflows
View already parsed workflows here or click here to add your own
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exome alignment and somatic variant detection for cle purpose
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Path: definitions/pipelines/somatic_exome_cle.cwl Branch/Commit ID: master |
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trnascan_wnode and gpx_qdump combined
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Path: bacterial_trna/wf_scan_and_dump.cwl Branch/Commit ID: test |
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CODEX analysis pipeline using Cytokit
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Path: steps/ometiff_second_stitching.cwl Branch/Commit ID: 1c73942 |
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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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Trim and reformat reads (single and paired end version)
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Path: workflows/trim_and_reformat_reads.cwl Branch/Commit ID: master |
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rna annotation
RNAs - predict, cluster, identify, annotate |
Path: CWL/Workflows/rna-annotation.workflow.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: ca6ca613 |
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io-int-default-wf.cwl
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Path: v1.0/v1.0/io-int-default-wf.cwl Branch/Commit ID: master |
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trimmed_fastq
Quality Control (raw data), Raw Data trimming and Quality Control (pre-processed) |
Path: structuralvariants/cwl/abstract_operations/subworkflows/trimmed_fastq.cwl Branch/Commit ID: master |
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cnv_codex
CNV CODEX calling |
Path: structuralvariants/cwl/subworkflows/cnv_codex.cwl Branch/Commit ID: 1.0.5 |
