Comparative analysis of de novo transcriptome assembly

查看全文 作　　者：CLARKE [1]Kaitlin;YANG [1,2]Yi;MARSH [2]Ronald;XIE [3]LingLin;ZHANG Ke [1]K.

机构地区：[1]Bioinformatics Core,Department of Pathology,University of North Dakota;[2]Department of Computer Science,University of North Dakota;[3]Department of Biochemistry and Molecular Biology,University of North Dakota

出　　处：《Science China(Life Sciences)》索引2013年第56卷第2期,共7页

基　　金：supported by grants from the National Center for Research Resources (5P20RR016471-12);the National Institute of General Medical Sciences (8 P20 GM103442-12) from the National Institutes of Health;the seed collaborative research grant from the Odegard School of Aerospace Sciences and the School of Medicine and Health Sciences at University of North Dakota 摘　　要：The fast development of next-generation sequencing technology presents a major computational challenge for data processing and analysis.A fast algorithm,de Bruijn graph has been successfully used for genome DNA de novo assembly;nevertheless,its performance for transcriptome assembly is unclear.In this study,we used both simulated and real RNA-Seq data,from either artificial RNA templates or human transcripts,to evaluate five de novo assemblers,ABySS,Mira,Trinity,Velvet and Oases.Of these assemblers,ABySS,Trinity,Velvet and Oases are all based on de Bruijn graph,and Mira uses an overlap graph algorithm.Various numbers of RNA short reads were selected from the External RNA Control Consortium(ERCC) data and human chromosome 22.A number of statistics were then calculated for the resulting contigs from each assembler.Each experiment was repeated multiple times to obtain the mean statistics and standard error estimate.Trinity had relative good performance for both ERCC and human data,but it may not consistently generate full length transcripts.ABySS was the fastest method but its assembly quality was low.Mira gave a good rate for mapping its contigs onto human chromosome 22,but its computational speed is not satisfactory.Our results suggest that transcript assembly remains a challenge problem for bioinformatics society.Therefore,a novel assembler is in need for assembling transcriptome data generated by next generation sequencing technique. 关键词：转录组组装 BRUIJN图 22号染色体装配质量基因组DNA 三位一体测序技术

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Comparative analysis of de novo transcriptome assembly

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