Yuki Endo, Fubito Toyama, C. Chiba, H. Mori, K. Shoji
{"title":"A Memory Efficient Short Read De Novo Assembly Algorithm","authors":"Yuki Endo, Fubito Toyama, C. Chiba, H. Mori, K. Shoji","doi":"10.2197/IPSJTBIO.8.2","DOIUrl":null,"url":null,"abstract":": Sequencing the whole genome of various species has many applications, not only in understanding bio- logical systems, but also in medicine, pharmacy, and agriculture. In recent years, the emergence of high-throughput next generation sequencing technologies has dramatically reduced the time and costs for whole genome sequencing. These new technologies provide ultrahigh throughput with a lower per-unit data cost. However, the data are generated from very short fragments of DNA. Thus, it is very important to develop algorithms for merging these fragments. One method of merging these fragments without using a reference dataset is called de novo assembly. Many algorithms for de novo assembly have been proposed in recent years. Velvet and SOAPdenovo2 are well-known assembly algorithms, which have good performance in terms of memory and time consumption. However, memory consumption increases dramatically when the size of input fragments is larger. Therefore, it is necessary to develop an alternative algorithm with low memory usage. In this paper, we propose an algorithm for de novo assembly with lower memory. In our experiments using E.coli K-12 strain MG 1655 and human chromosome 14, the memory consumption of our proposed algorithm was less than that of other popular assemblers.","PeriodicalId":38959,"journal":{"name":"IPSJ Transactions on Bioinformatics","volume":"8 1","pages":"2-8"},"PeriodicalIF":0.0000,"publicationDate":"2015-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.2197/IPSJTBIO.8.2","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"IPSJ Transactions on Bioinformatics","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.2197/IPSJTBIO.8.2","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"Biochemistry, Genetics and Molecular Biology","Score":null,"Total":0}
引用次数: 0
Abstract
: Sequencing the whole genome of various species has many applications, not only in understanding bio- logical systems, but also in medicine, pharmacy, and agriculture. In recent years, the emergence of high-throughput next generation sequencing technologies has dramatically reduced the time and costs for whole genome sequencing. These new technologies provide ultrahigh throughput with a lower per-unit data cost. However, the data are generated from very short fragments of DNA. Thus, it is very important to develop algorithms for merging these fragments. One method of merging these fragments without using a reference dataset is called de novo assembly. Many algorithms for de novo assembly have been proposed in recent years. Velvet and SOAPdenovo2 are well-known assembly algorithms, which have good performance in terms of memory and time consumption. However, memory consumption increases dramatically when the size of input fragments is larger. Therefore, it is necessary to develop an alternative algorithm with low memory usage. In this paper, we propose an algorithm for de novo assembly with lower memory. In our experiments using E.coli K-12 strain MG 1655 and human chromosome 14, the memory consumption of our proposed algorithm was less than that of other popular assemblers.
对各种物种的全基因组进行测序不仅在理解生物系统方面有许多应用,而且在医学、制药和农业方面也有许多应用。近年来,高通量下一代测序技术的出现大大降低了全基因组测序的时间和成本。这些新技术以更低的单位数据成本提供了超高的吞吐量。然而,这些数据是由非常短的DNA片段生成的。因此,开发融合这些碎片的算法是非常重要的。在不使用参考数据集的情况下合并这些片段的一种方法称为de novo assembly。近年来提出了许多新的从头组装算法。Velvet和SOAPdenovo2是众所周知的汇编算法,它们在内存和时间消耗方面具有良好的性能。但是,当输入片段的大小较大时,内存消耗会急剧增加。因此,有必要开发一种低内存占用的替代算法。本文提出了一种低内存的从头组装算法。在大肠杆菌K-12菌株MG 1655和人类14号染色体的实验中,我们提出的算法的内存消耗低于其他流行的汇编程序。