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BASE: A Practical de novo Assembler for Large Genomes Using Longer NGS Reads

机译:BASE:使用较长的NGS读物的大型基因组实用de novo汇编程序

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De novo genome assembly is a fundamental problem in genomic research. When assembling relatively large genomes, time is often a very important concern, and one might have no choice but to use a more efficient assembler like SOAPdenovo2 instead of a high-quality but prohibitively slow assembler (SPAdes is a typical example). As the read length of high-throughput sequencers increases beyond lOObp, it has been expected that the quality issue of SOAPdenov2 can gradually improve. Yet SOAPdenov2, a typical de Bruijn graph based assembler, has inherent difficulty to fully utilize the advantage of longer reads (say, 150 bp and 250 bp from Illumina HiSeq and MiSeq, respectively). Other assemblers, such as the string graph assembler SGA and the multisized de Bruijn graph assembler SPAdes, though more favorable for longer reads, are very slow and less popular. It is still up to the challenge how to better utilize longer reads to develop a fast-and-accurate assembler.
机译:从头进行基因组组装是基因组研究中的一个基本问题。当组装相对较大的基因组时,时间通常是一个非常重要的问题,人们可能别无选择,只能使用像SOAPdenovo2这样的更高效的汇编器来代替高质量但过慢的汇编器(SPAdes是一个典型的例子)。随着高通量测序仪的读取长度增加到超过100bp,可以预期SOAPdenov2的质量问题会逐渐改善。然而,SOAPdenov2是典型的基于de Bruijn图的汇编程序,具有固有的困难,难以充分利用较长读取的优势(例如,分别来自Illumina HiSeq和MiSeq的150 bp和250 bp)。其他汇编程序,例如字符串图形汇编程序SGA和多尺寸的de Bruijn图形汇编程序SPAdes,尽管更适合较长的读取时间,但它们的运行速度很慢且不那么受欢迎。如何更好地利用更长的读取时间来开发快速而准确的汇编程序,仍然是一个挑战。

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