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RNA-Skim: a rapid method for RNA-Seq quantification at transcript level

机译:RNA-Skim:在转录水平上定量RNA-Seq的快速方法

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Motivation: RNA-Seq technique has been demonstrated as a revolutionary means for exploring transcriptome because it provides deep coverage and base pair-level resolution. RNA-Seq quantification is proven to be an efficient alternative to Microarray technique in gene expression study, and it is a critical component in RNA-Seq differential expression analysis. Most existing RNA-Seq quantification tools require the alignments of fragments to either a genome or a transcriptome, entailing a time-consuming and intricate alignment step. To improve the performance of RNA-Seq quantification, an alignment- free method, Sailfish, has been recently proposed to quantify transcript abundances using all k-mers in the transcriptome, demonstrating the feasibility of designing an efficient alignment-free method for transcriptome quantification. Even though Sailfish is substantially faster than alternative alignment-dependent methods such as Cufflinks, using all k-mers in the transcriptome quantification impedes the scalability of the method. Results: We propose a novel RNA-Seq quantification method, RNA-Skim, which partitions the transcriptome into disjoint transcript clusters based on sequence similarity, and introduces the notion of sig-mers, which are a special type of k-mers uniquely associated with each cluster. We demonstrate that the sig-mer counts within a cluster are sufficient for estimating transcript abundances with accuracy comparable with any state-of-the-art method. This enables RNA-Skim to perform transcript quantification on each cluster independently, reducing a complex optimization problem into smaller optimization tasks that can be run in parallel. As a result, RNA-Skim uses <4% of the k-mers and <10% of the CPU time required by Sailfish. It is able to finish transcriptome quantification in <10 min per sample by using just a single thread on a commodity computer, which represents >100 speedup over the state-of-the-art alignment-based methods, while delivering comparable or higher accuracy.
机译:动机:RNA-Seq技术已被证明是探索转录组的一种革命性手段,因为它提供了深度覆盖和碱基对水平的分辨率。 RNA-Seq定量已被证明是基因表达研究中微阵列技术的有效替代方法,并且是RNA-Seq差异表达分析中的关键组成部分。大多数现有的RNA-Seq定量工具都需要将片段与基因组或转录组进行比对,这需要耗时且复杂的比对步骤。为了提高RNA-Seq定量的性能,最近提出了一种无比对方法,Sailfish,用于使用转录组中的所有k-mer定量转录本丰度,证明了设计一种有效的无比对方法进行转录组定量的可行性。尽管Sailfish的速度大大快于其他依赖比对的依赖方法,例如袖扣,但在转录组定量中使用所有k-mers却阻碍了该方法的可扩展性。结果:我们提出了一种新颖的RNA-Seq定量方法RNA-Skim,该方法基于序列相似性将转录组划分为不相交的转录本簇,并引入了sig-mers概念,它是一种独特的与k-mers相关的特殊类型每个集群。我们证明了群集中的信号计数足以估算转录本丰度,其准确性可与任何最新方法媲美。这使RNA-Skim能够独立地在每个簇上执行转录本定量,从而将复杂的优化问题减少为可以并行运行的较小的优化任务。结果,RNA-Skim使用了Sailfish所需的k-mers的<4%和CPU时间的<10%。只需使用商用计算机上的单个线程,就可以在每个样品中用不到10分钟的时间完成转录组的定量分析,这表示与基于最新比对方法的方法相比,其提速超过100倍,同时提供了相当或更高的准确性。

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