Latest version of vSNP see vSNP3 repository.
Whole genome sequencing for disease tracing and outbreak investigations is routinely required for high consequence diseases. vSNP is an accreditation-friendly and robust tool, designed for easy error correction and SNP validation. vSNP rapidly generates annotated SNP tables and corresponding phylogenetic trees that can be easily scaled for reporting purposes. It is able to process large scale datasets, and efficiently accommodates multiple references.
- Allows for the creation of customized groups utilizing user specified SNPs.
- Functionality to filter desired SNP positions by group or for all groups.
- Two types of output:
- A spreadsheet, or SNP table containing SNP calls sorted in evolutionary order with annotation and genome position information.
- Corresponding phylogenetic trees
- Ability for run-detail to be provided and optimized by multiple users.
vSNP is a 2-step process for efficiency.
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vSNP_step1.pytakes as input single or paired FASTQ files and either a reference FASTA or directory name containing the reference FASTA (see vsnp_path_adder.py below). For Mycobacterium tuberculosis complex and Brucella species, if no FASTA file or directory name is provided a "best reference" is automatically selectedNOTE: It is only necessary to process each set of raw data once for each reference. The VCF file from Step 1 is saved for future analyses with additional samples in Step 2. It is recommended that VCF files generated with a single reference be placed in a single directory to facilitate future analysis. Only VCF files generated from the same reference can be compared in Step 2.
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vSNP_step2.pybuilds SNP tables and corresponding phylogenetic trees from a directory containing a collection of zc.vcf files output from step 1. Step 2 will handle large datasets with thousands of VCF files, outputting detailed comparisons in minutes.
It is expected the setup user is familiar with the command-line and can install conda.
Do not work in base. If needed make new environmnet.
conda create --name myenvInstallation:
conda install vsnp -c conda-forge -c biocondaRun vSNP_step1.py -h to see usage details.
macOS users may need to follow these special instructions for Samtools.
Except for a reference FASTA file, no other dependency file is required to run vSNP. However, other files are recommended to add additional functionality to the script. For example, Excel file containing defining SNPs and filters will allow for the creation of custom subgroups. A template is provided at dependencies/template_defining_filter.xlsx.
Download and add reference options. It is recommended that reference options be placed on storage accessible to both computing resources and subject matter experts analyzing the output data.
git clone https://github.com/USDA-VS/vSNP_reference_options.gitUse vsnp_path_adder.py to add options. See vsnp_path_adder.py -h for help.
For example, after running the following all subdirectories are accessible using the -r option.
vsnp_path_adder.py -d /full/path/to/vSNP_referenece_options
vSNP_step1.py -r1 *_R1*gz -r2 *_R2*gz -r Mycobacterium_AF2122Download test files:
git clone https://github.com/USDA-VS/fastq_data_set-tb_complexPlace each sample in its own directory, and on each directory run the following command:
vSNP_step1.py -r1 *_R1*gz -r2 *_R2*gzSee help running multiple samples at once.
Copy *zc.vcf output from step 1 into a directory for step 2. Only samples compared to the same reference can be analyzed together in step 2.
Run vSNP_step2.py on this directory.
As with reference options, it is recommended to place output from step 1 and 2 on storage accessible to subject matter experts analyzing the data. It may be necessary to use data from all three sources- reference options, step 1 and step 2 to fully understand the relationships of the data.
Recommended directory structure for step 1 and 2 output:
Procedure detail is here.
vSNP utility scripts.
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