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DASH: localising dynamic programming for order of magnitude faster, accurate sequence alignment

机译:DASH:定位动态编程,尺寸更快,准确顺序对齐

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In this paper we present our genomic and proteomic sequence alignment algorithm, DASH, which results in order of magnitude speed improvement when compared to NCBI-BLAST 2.2.6, with superior sensitivity. Dynamic programming (DP) is the predominant contributor to search time for algorithms such as BLAST and FastA/P. Improving the efficiency of DP provides an opportunity to increase sensitivity, or significantly reduce search times and help offset the effects of the continuing exponential growth in database sizes. Specifically, for nucleotide searching we have demonstrated an order of magnitude speed improvement with significantly improved sensitivity, or alternatively moderate speed up with further sensitivity gains, depending on the parameters selected. Smith-Waterman complete DP is used as the sensitivity benchmark. Similar speed and sensitivity results are presented for protein searching. Since our algorithm is highly parallel, we have developed dedicated hardware which we will present in a companion paper, and a distributed version of our software (DDASH), which we expect to provide linear speedup on a cluster.
机译:在本文中,我们介绍了我们的基因组和蛋白质组学序列对准算法,该序列,其导致与NCBI-Blast 2.2.6相比的幅度速度改善的顺序,具有优异的敏感性。动态编程(DP)是搜索算法的主要贡献者,例如Blast和Fasta / p。提高DP的效率提供了增加灵敏度的机会,或者显着降低搜索时间,并帮助抵消持续指数增长在数据库大小中的影响。具体地,对于核苷酸搜索,我们已经证明了一种幅度速度改善的顺序,并且根据所选择的参数,以显着提高的灵敏度改善,或者以进一步的敏感性增长。 Smith-Waterman Complete DP用作灵敏度基准。呈现类似的速度和灵敏度结果用于蛋白质搜索。由于我们的算法很平行,我们开发了我们将在伴侣论文中呈现的专用硬件以及我们希望在群集中提供线性加速的软件(DDash)中的专用硬件。

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