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首页> 外文期刊>Genome research >De novo fragment assembly with short mate-paired reads: Does the read length matter?
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De novo fragment assembly with short mate-paired reads: Does the read length matter?

机译:短配对配对读取的从头片段组装:读取长度重要吗?

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Increasing read length is currently viewed as the crucial condition for fragment assembly with next-generation sequencing technologies. However, introducing mate-paired reads (separated by a gap of length, GapLength) opens a possibility to transform short mate-pairs into long mate-reads of length approximately GapLength, and thus raises the question as to whether the read length (as opposed to GapLength) even matters. We describe a new tool, EULER-USR, for assembling mate-paired short reads and use it to analyze the question of whether the read length matters. We further complement the ongoing experimental efforts to maximize read length by a new computational approach for increasing the effective read length. While the common practice is to trim the error-prone tails of the reads, we present an approach that substitutes trimming with error correction using repeat graphs. An important and counterintuitive implication of this result is that one may extend sequencing reactions that degrade with length "past their prime" to where the error rate grows above what is normally acceptable for fragment assembly.
机译:当前,增加读取长度被视为下一代测序技术进行片段组装的关键条件。但是,引入配对配对的读取(由长度间隔GapLength分隔)可以将短配对配对转换为长度约为GapLength的长配对读取,因此引发了一个问题,即读取长度(相对于对GapLength而言)。我们描述了一种新的工具EULER-USR,用于组装配对配对的短读物,并使用它来分析读长是否重要的​​问题。我们通过增加有效读取长度的新计算方法进一步补充了正在进行的实验工作,以最大化读取长度。虽然通常的做法是修整读取中容易出错的尾部,但我们提出了一种方法,该方法可以使用重复图来代替修整并进行纠错。此结果的一个重要且与直觉相反的含义是,随着长度“过去”的延长,测序反应可能会延伸到错误率超过片段装配通常可接受的水平。

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