Workflow to detect SNV from Illumina sequenced baculovirus isolates
variant-analysis-baculovirus-isolate-variation/workflow-to-detect-snv-from-illumina-sequenced-baculovirus-isolates
Launch in Tutorial Mode
question
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galaxy-download Download
flowchart TD 0["Download reference genome in FASTA format from NCBI"]; 1["Paired dataset collection in FASTQ format downloaded from NCBI SRA"]; 2["Collapse Genbank file"]; 0 -->|output| 2; 3["Trim Galore!"]; 1 -->|list_paired| 3; 4["Rename reference genome sequence header"]; 2 -->|output| 4; 5["Map with BWA-MEM"]; 3 -->|trimmed_reads_paired_collection| 5; 4 -->|outfile| 5; 6["bcftools mpileup"]; 5 -->|bam_output| 6; 4 -->|outfile| 6; 7["bcftools call"]; 6 -->|output_file| 7; d8a45d4f-c8e4-40da-ba84-7ec13aa8ca4d["Output\nbcftools_call_output"]; 7 --> d8a45d4f-c8e4-40da-ba84-7ec13aa8ca4d; style d8a45d4f-c8e4-40da-ba84-7ec13aa8ca4d stroke:#2c3143,stroke-width:4px; 8["VCF Transformation"]; 7 -->|output_file| 8; 9["Relative allele frequency calculation"]; 8 -->|out_file1| 9; 10["Replace Text"]; 9 -->|outfile| 10; 186d4e5c-fceb-4031-b569-d84dbcd1c156["Output\nvcf_table"]; 10 --> 186d4e5c-fceb-4031-b569-d84dbcd1c156; style 186d4e5c-fceb-4031-b569-d84dbcd1c156 stroke:#2c3143,stroke-width:4px; 11["Reduce dataset to ALT1"]; 10 -->|outfile| 11; 7ebeb330-a4df-4027-b636-daa0e5e39938["Output\nvcf_table_ALT1"]; 11 --> 7ebeb330-a4df-4027-b636-daa0e5e39938; style 7ebeb330-a4df-4027-b636-daa0e5e39938 stroke:#2c3143,stroke-width:4px; 12["SNV plot"]; 11 -->|out_file1| 12; 13["SNV specificity calculation"]; 11 -->|out_file1| 13; b2f9dabd-7bbf-4b96-a351-78a2b2552586["Output\nvcf_table_ALT1_specificity"]; 13 --> b2f9dabd-7bbf-4b96-a351-78a2b2552586; style b2f9dabd-7bbf-4b96-a351-78a2b2552586 stroke:#2c3143,stroke-width:4px; 14["Filter"]; 13 -->|outfile| 14; 15["Filter"]; 13 -->|outfile| 15; 16["Filter"]; 13 -->|outfile| 16; 17["ggplot2 V15 dotplot "]; 14 -->|out_file1| 17; 18["ggplot2 CpGV-S dotplot"]; 15 -->|out_file1| 18; 19["ggplot2 CpGV-E2 dotplot"]; 16 -->|out_file1| 19;
Inputs
Input | Label |
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Outputs
From | Output | Label |
---|---|---|
toolshed.g2.bx.psu.edu/repos/iuc/bcftools_call/bcftools_call/1.15.1+galaxy5 | bcftools call | |
toolshed.g2.bx.psu.edu/repos/bgruening/text_processing/tp_replace_in_column/9.3+galaxy1 | Replace Text | |
Filter1 | Filter | Reduce dataset to ALT1 |
toolshed.g2.bx.psu.edu/repos/bgruening/text_processing/tp_awk_tool/9.3+galaxy1 | Text reformatting | SNV specificity calculation |
Tools
To use these workflows in Galaxy you can either click the links to download the workflows, or you can right-click and copy the link to the workflow which can be used in the Galaxy form to import workflows.
Importing into Galaxy
Below are the instructions for importing these workflows directly into your Galaxy server of choice to start using them!Hands On: Importing a workflow
- Click on Workflow on the top menu bar of Galaxy. You will see a list of all your workflows.
- Click on galaxy-upload Import at the top-right of the screen
- Provide your workflow
- Option 1: Paste the URL of the workflow into the box labelled “Archived Workflow URL”
- Option 2: Upload the workflow file in the box labelled “Archived Workflow File”
- Click the Import workflow button
Below is a short video demonstrating how to import a workflow from GitHub using this procedure:
Video: Importing a workflow from URL
Version History
Version | Commit | Time | Comments |
---|---|---|---|
1 | d8824c6c2 | 2025-01-30 15:19:15 | Workflow test data added. |
For Admins
Installing the workflow tools
wget https://training.galaxyproject.org/training-material/topics/variant-analysis/tutorials/baculovirus-isolate-variation/workflows/Workflow-to-detect-SNV-from-Illumina-sequenced-baculovirus-isolates.ga -O workflow.ga workflow-to-tools -w workflow.ga -o tools.yaml shed-tools install -g GALAXY -a API_KEY -t tools.yaml workflow-install -g GALAXY -a API_KEY -w workflow.ga --publish-workflows