| Literature DB >> 33598139 |
Kristoffer Sahlin1, Marisa C W Lim2, Stefan Prost3,4.
Abstract
Third-generation sequencing technologies, such as Oxford Nanopore Technologies (ONT) and Pacific Biosciences (PacBio), have gained popularity over the last years. These platforms can generate millions of long-read sequences. This is not only advantageous for genome sequencing projects, but also advantageous for amplicon-based high-throughput sequencing experiments, such as DNA barcoding. However, the relatively high error rates associated with these technologies still pose challenges for generating high-quality consensus sequences. Here, we present NGSpeciesID, a program which can generate highly accurate consensus sequences from long-read amplicon sequencing technologies, including ONT and PacBio. The tool includes clustering of the reads to help filter out contaminants or reads with high error rates and employs polishing strategies specific to the appropriate sequencing platform. We show that NGSpeciesID produces consensus sequences with improved usability by minimizing preprocessing and software installation and scalability by enabling rapid processing of hundreds to thousands of samples, while maintaining similar consensus accuracy as current pipelines.Entities:
Keywords: DNA barcoding; amplicon sequencing; sequence clustering; third‐generation sequencing
Year: 2021 PMID: 33598139 PMCID: PMC7863402 DOI: 10.1002/ece3.7146
Source DB: PubMed Journal: Ecol Evol ISSN: 2045-7758 Impact factor: 2.912