Workflow Type: Galaxy
Frozen
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. |
|
| Short-reads | #main/Short-reads | Short-reads as a paired-end collection of fastqsanger(.gz) files |
|
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 |
|
| Contamination Filtered Reads | #main/Contamination Filtered Reads | n/a |
|
| MultiQC HTML Report | #main/MultiQC HTML Report | n/a |
|
Version History
v0.1 (earliest) Created 6th Dec 2025 at 03:02 by WorkflowHub Bot
Updated to v0.1
Frozen
v0.1
25561f7
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Views: 1111 Downloads: 3573 Runs: 2
Created: 6th Dec 2025 at 03:01
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https://orcid.org/0000-0001-9852-1987