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MapSplice: Accurate mapping of RNA-seq reads for splice junction discovery

机译:MapSplice:准确绘制RNA-seq读数以进行剪接连接发现

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摘要

The accurate mapping of reads that span splice junctions is a critical component of all analytic techniques that work with RNA-seq data. We introduce a second generation splice detection algorithm, MapSplice, whose focus is high sensitivity and specificity in the detection of splices as well as CPU and memory efficiency. MapSplice can be applied to both short (<75 bp) and long reads (≥75 bp). MapSplice is not dependent on splice site features or intron length, consequently it can detect novel canonical as well as non-canonical splices. MapSplice leverages the quality and diversity of read alignments of a given splice to increase accuracy. We demonstrate that MapSplice achieves higher sensitivity and specificity than TopHat and SpliceMap on a set of simulated RNA-seq data. Experimental studies also support the accuracy of the algorithm. Splice junctions derived from eight breast cancer RNA-seq datasets recapitulated the extensiveness of alternative splicing on a global level as well as the differences between molecular subtypes of breast cancer. These combined results indicate that MapSplice is a highly accurate algorithm for the alignment of RNA-seq reads to splice junctions. Software download URL: http://www.netlab.uky.edu/p/bioinfo/MapSplice.
机译:跨剪接点的读段的准确映射是使用RNA-seq数据的所有分析技术的关键组成部分。我们引入了第二代接头检测算法MapSplice,其重点是在接头检测以及CPU和内存效率方面的高灵敏度和特异性。 MapSplice可以应用于短读(<75 bp)和长读(≥75bp)。 MapSplice不依赖于剪接位点特征或内含子长度,因此它可以检测新的正则和非正则剪接。 MapSplice利用给定接头的读取对齐方式的质量和多样性来提高准确性。我们证明,在一组模拟RNA序列数据上,MapSplice比TopHat和SpliceMap具有更高的灵敏度和特异性。实验研究也支持该算法的准确性。来自八个乳腺癌RNA-seq数据集的剪接连接点概括了全球范围内可变剪接的广泛性以及乳腺癌分子亚型之间的差异。这些合并的结果表明,MapSplice是用于将RNA-seq读数与剪接点对齐的高精度算法。软件下载URL:http://www.netlab.uky.edu/p/bioinfo/MapSplice。

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