Workflow Type: Galaxy

This workflow takes paired-end Illumina fastq(.gz) files and runs Bowtie to map the reads against a reference genome (human, by default) and keep only the reads that do not align. MultiQC is used to aggregate the mapping reports.

Inputs

ID Name Description Type
Contaminant Reference Genome #main/Host/Contaminant Reference Genome Reads not mapping to this reference genome will be kept.
  • string
Short-reads #main/Short-reads Short-reads as a paired-end collection of fastqsanger(.gz) files
  • array containing
    • File

Steps

ID Name Description
2 Bowtie2 Map the reads against a reference genome and output the ones not mapping the reference genome toolshed.g2.bx.psu.edu/repos/devteam/bowtie2/bowtie2/2.5.4+galaxy0
3 MultiQC Aggregation of the mapping statistics for all samples toolshed.g2.bx.psu.edu/repos/iuc/multiqc/multiqc/1.33+galaxy0

Outputs

ID Name Description Type
Bowtie2 Mapping Statistics #main/Bowtie2 Mapping Statistics n/a
  • File
Contamination Filtered Reads #main/Contamination Filtered Reads n/a
  • File
MultiQC HTML Report #main/MultiQC HTML Report n/a
  • File

Version History

v0.3 (latest) Created 21st Jan 2026 at 03:01 by WorkflowHub Bot

Updated to v0.3


Frozen v0.3 cb3aedc

v0.2 Created 9th Dec 2025 at 03:02 by WorkflowHub Bot

Updated to v0.2


Frozen v0.2 db6c354

v0.1 (earliest) Created 6th Dec 2025 at 03:02 by WorkflowHub Bot

Updated to v0.1


Frozen v0.1 25561f7
help Creators and Submitter
Activity

Views: 1111   Downloads: 3573   Runs: 2

Created: 6th Dec 2025 at 03:01

help Tags

This item has not yet been tagged.

help Attributions

None

Total size: 20.8 KB
Powered by
(v.1.17.3)
Copyright © 2008 - 2026 The University of Manchester and HITS gGmbH