This pipeline and toolkit is used to detect and analyze single nucleotide differences between closely related bacterial isolates.
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Noteable features
- Avoids false-negative mutations due to low coverage; if a mutation is found in at least one isolate in a set, the evidence at that position will be investigated to make a best-guess call.
- Avoids false-positives mutations by facilitating visualization of raw data, across samples (whereas pileup formats must be investigated on a sample-by-sample basis) and changing of threshold to best fit your use case.
- Enables easy evolutionary analysis, including phylogenetic construction, nonsynonmous vs synonymous mutation counting, and parallel evolution
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Inputs (to Snakemake cluster step):
- short-read sequencing data of closely related bacterial isolates
- an annotated reference genome
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Outputs (of local analysis step):
- table of high-quality SNVs that differentiate isolates from each other
- parsimony tree of how the isolates are related to each other
The pipeline is split into two main components, as described below. A complete tutorial can be found at the bottom of this page.
The first portion of WideVariant aligns raw sequencing data from bacterial isolates to a reference genome, identifies candidate SNV positions, and creates useful data structure for supervised local data filtering. This step is implemented in a workflow management system called Snakemake and is executed on a SLURM cluster. More information is available here.
The second portion of WideVariant filters candidate SNVs based on data arrays generated in the first portion and generates a high-quality SNV table and a parsimony tree. This step is implemented with a custom python script. More information can be found here.
Main WideVariant pipeline README
Previous iterations of this pipeline have been used to study: