Rapid genotyping of targeted viral samples using Illumina short-read sequencing data.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 36112576.
- Also identified by DOI 10.1371/journal.pone.0274414 and PMC identifier 9481040.
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Abstract
The most important information about microorganisms might be their accurate genome sequence. Using current Next Generation Sequencing methods, sequencing data can be generated at an unprecedented pace. However, we still lack tools for the automated and accurate reference-based genotyping of viral sequencing reads. This paper presents our pipeline designed to reconstruct the dominant consensus genome of viral samples and analyze their within-host variability. We benchmarked our approach on numerous datasets and showed that the consensus genome of samples could be obtained reliably without further manual data curation. Our pipeline can be a valuable tool for fast identifying viral samples. The pipeline is publicly available on the project's GitHub page (https://github.com/laczkol/QVG).
Medical subject headings
- High-Throughput Nucleotide Sequencing
- Software