deBGA: read alignment with de Bruijn graph-based seed and extension

被引:43
|
作者
Liu, Bo [1 ]
Guo, Hongzhe [1 ]
Brudno, Michael [2 ,3 ,4 ]
Wang, Yadong [1 ]
机构
[1] Harbin Inst Technol, Ctr Bioinformat, Harbin 150001, Heilongjiang, Peoples R China
[2] Univ Toronto, Dept Comp Sci, Toronto, ON M5S 3G4, Canada
[3] Hosp Sick Children, Genet & Genome Biol Program, Toronto, ON M5G 1L7, Canada
[4] Hosp Sick Children, Ctr Computat Med, Toronto, ON M5G 1L7, Canada
关键词
ACCURATE; SEQUENCE; GENOMES;
D O I
10.1093/bioinformatics/btw371
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Motivation: As high-throughput sequencing (HTS) technology becomes ubiquitous and the volume of data continues to rise, HTS read alignment is becoming increasingly rate-limiting, which keeps pressing the development of novel read alignment approaches. Moreover, promising novel applications of HTS technology require aligning reads to multiple genomes instead of a single reference; however, it is still not viable for the state-of-the-art aligners to align large numbers of reads tomultiple genomes. Results: We propose de Bruijn Graph-based Aligner (deBGA), an innovative graph-based seedand- extension algorithm to align HTS reads to a reference genome that is organized and indexed using a de Bruijn graph. With its well-handling of repeats, deBGA is substantially faster than stateof- the-art approaches while maintaining similar or higher sensitivity and accuracy. This makes it particularly well-suited to handle the rapidly growing volumes of sequencing data. Furthermore, it provides a promising solution for aligning reads to multiple genomes and graph-based references in HTS applications.
引用
收藏
页码:3224 / 3232
页数:9
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