| Literature DB >> 33436980 |
Pierre Morisse1, Camille Marchet2, Antoine Limasset2, Thierry Lecroq3, Arnaud Lefebvre3.
Abstract
Third-generation sequencing technologies allow to sequence long reads of tens of kbp, that are expected to solve various problems. However, they display high error rates, currently capped around 10%. Self-correction is thus regularly used in long reads analysis projects. We introduce CONSENT, a new self-correction method that relies both on multiple sequence alignment and local de Bruijn graphs. To ensure scalability, multiple sequence alignment computation benefits from a new and efficient segmentation strategy, allowing a massive speedup. CONSENT compares well to the state-of-the-art, and performs better on real Oxford Nanopore data. Specifically, CONSENT is the only method that efficiently scales to ultra-long reads, and allows to process a full human dataset, containing reads reaching up to 1.5 Mbp, in 10 days. Moreover, our experiments show that error correction with CONSENT improves the quality of Flye assemblies. Additionally, CONSENT implements a polishing feature, allowing to correct raw assemblies. Our experiments show that CONSENT is 2-38x times faster than other polishing tools, while providing comparable results. Furthermore, we show that, on a human dataset, assembling the raw data and polishing the assembly is less resource consuming than correcting and then assembling the reads, while providing better results. CONSENT is available at https://github.com/morispi/CONSENT .Entities:
Year: 2021 PMID: 33436980 PMCID: PMC7804095 DOI: 10.1038/s41598-020-80757-5
Source DB: PubMed Journal: Sci Rep ISSN: 2045-2322 Impact factor: 4.379