Abstract | ||
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The third-generation sequencing technology has advanced genome analysis with long-read length, but the reads need error correction due to the high error rate. Error correction is a time-consuming process especially when the sequencing coverage is high. Generally, for a pair of overlapping reads A and B, the existing error correction methods perform a base-level alignment from B to A when correcting the read A. And another base-level alignment from A to B is performed when correcting the read B. However, based on our observation, the base-level alignment information can be reused. In this article, we present a fast error correction tool Fec, using two-rounds overlapping and caching. Fec can be used independently or as an error correction step in an assembly pipeline. In the first round, Fec uses a large window size (20) to quickly find enough overlaps to correct most of the reads. In the second round, a small window size (5) is used to find more overlaps for the reads with insufficient overlaps in the first round. When performing base-level alignment, Fec searches the cache first. If the alignment exists in the cache, Fec takes this alignment out and deduces the second alignment from it. Otherwise, Fec performs base-level alignment and stores the alignment in the cache. We test Fec on nine datasets, and the results show that Fec has 1.24-38.56 times speed-up compared to MECAT, CANU and MINICNS on five PacBio datasets and 1.16-27.8 times speed-up compared to NECAT and CANU on four nanopore datasets. |
Year | DOI | Venue |
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2022 | 10.1093/bioinformatics/btac565 | BIOINFORMATICS |
DocType | Volume | Issue |
Journal | 38 | 19 |
ISSN | Citations | PageRank |
1367-4803 | 0 | 0.34 |
References | Authors | |
0 | 6 |
Name | Order | Citations | PageRank |
---|---|---|---|
Jun Zhang | 1 | 0 | 3.04 |
Fan Nie | 2 | 0 | 0.34 |
Neng Huang | 3 | 2 | 2.40 |
Peng Ni | 4 | 6 | 3.80 |
Feng Luo | 5 | 284 | 26.03 |
Jianxin Wang | 6 | 2163 | 283.94 |