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Parallel and Scalable Short-Read Alignment on Multi-Core Clusters Using UPC++

机译:使用UPC ++在多核群集上进行并行和可扩展的短读对齐

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摘要

The growth of next-generation sequencing (NGS) datasets poses a challenge to the alignment of reads to reference genomes in terms of alignment quality and execution speed. Some available aligners have been shown to obtain high quality mappings at the expense of long execution times. Finding fast yet accurate software solutions is of high importance to research, since availability and size of NGS datasets continue to increase. In this work we present an efficient parallelization approach for NGS short-read alignment on multi-core clusters. Our approach takes advantage of a distributed shared memory programming model based on the new UPC++ language. Experimental results using the CUSHAW3 aligner show that our implementation based on dynamic scheduling obtains good scalability on multi-core clusters. Through our evaluation, we are able to complete the single-end and paired-end alignments of 246 million reads of length 150 base-pairs in 11.54 and 16.64 minutes, respectively, using 32 nodes with four AMD Opteron 6272 16-core CPUs per node. In contrast, the multi-threaded original tool needs 2.77 and 5.54 hours to perform the same alignments on the 64 cores of one node. The source code of our parallel implementation is publicly available at the CUSHAW3 homepage ().
机译:下一代测序(NGS)数据集的增长对比对质量和执行速度方面的读取与参考基因组比对提出了挑战。已显示一些可用的对齐器以较长的执行时间为代价获得高质量的映射。由于NGS数据集的可用性和规模不断增加,因此找到快速而准确的软件解决方案对于研究至关重要。在这项工作中,我们提出了一种有效的并行化方法,用于多核群集上的NGS短读对齐。我们的方法利用了基于新的UPC ++语言的分布式共享内存编程模型。使用CUSHAW3对齐器的实验结果表明,我们基于动态调度的实现在多核群集上获得了良好的可伸缩性。通过我们的评估,我们能够使用32个节点,每个节点具有四个AMD Opteron 6272 16核CPU,分别在11.54和16.64分钟内完成长度为150个碱基对的2.46亿个读取的单端和双端比对。 。相比之下,多线程原始工具需要2.77和5.54小时才能在一个节点的64个内核上执行相同的对齐。我们的并行实现的源代码可在CUSHAW3主页()上公开获得。

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