Explore Workflows
View already parsed workflows here or click here to add your own
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bulk_analysis.cwl
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Path: steps/bulk_analysis.cwl Branch/Commit ID: 44dbe38 |
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bulk_analysis.cwl
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Path: steps/bulk_analysis.cwl Branch/Commit ID: 5465f66 |
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snapanalysis_setup_and_analyze.cwl
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Path: steps/snapanalysis_setup_and_analyze.cwl Branch/Commit ID: 302f1f3 |
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tRNA_selection.cwl
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Path: tools/tRNA_selection.cwl Branch/Commit ID: 8e196ab |
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EMG pipeline v3.0 (single end version)
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Path: workflows/emg-pipeline-v3.cwl Branch/Commit ID: 1b0851e |
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wf_calculate_models.cwl
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Path: yw_cwl_modeling/yw_cwl_parser_old/Examples/calculate_models/wf_calculate_models.cwl Branch/Commit ID: master |
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chromVAR scATAC-seq pipeline
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Path: chromvar-pipeline.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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Functional analyis of sequences that match the 16S SSU
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Path: workflows/16S_taxonomic_analysis.cwl Branch/Commit ID: master |
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CODEX analysis pipeline using Cytokit
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Path: pipeline.cwl Branch/Commit ID: 221f7c4 |
