UPC plus plus for Bioinformatics: A Case Study Using Genome-Wide Association Studies

被引:0
作者
Kaessens, Jan C. [1 ]
Gonzalez-Dominguez, Jorge [2 ]
Wienbrandt, Lars [1 ]
Schmidt, Bertil [2 ]
机构
[1] Christian Albrechts Univ Kiel, Dept Comp Sci, Kiel, Germany
[2] Johannes Gutenberg Univ Mainz, Parallel & Distributed Architectures Grp, Mainz, Germany
来源
2014 IEEE INTERNATIONAL CONFERENCE ON CLUSTER COMPUTING (CLUSTER) | 2014年
基金
英国惠康基金;
关键词
PGAS; UPC plus; GWAS; Bioinformatics; EPISTATIC INTERACTION DETECTION; GENE-GENE INTERACTIONS; CANCER SUSCEPTIBILITY; SNP INTERACTIONS; PAIR; TOOL;
D O I
暂无
中图分类号
TP3 [计算技术、计算机技术];
学科分类号
0812 ;
摘要
Modern genotyping technologies are able to obtain up to a few million genetic markers (such as SNPs) of an individual within a few minutes of time. Detecting epistasis, such as SNP-SNP interactions, in Genome-Wide Association Studies is an important but time-consuming operation since statistical computations have to be performed for each pair of measured markers. Therefore, a variety of HPC architectures have been used to accelerate these studies. In this work we present a parallel approach for multi-core clusters, which is implemented with UPC++ and takes advantage of the features available in the Partitioned Global Address Space and Object Oriented Programming models. Our solution is based on a well-known regression model (used by the popular BOOST tool) to test SNP-pairs interactions. Experimental results show that UPC++ is suitable for parallelizing data-intensive bioinformatics applications on clusters. For instance, it reduces the time to analyze a real-world dataset with more than 500,000 SNPs and 5,000 individuals from several days when using a single core to less than one minute using 512 nodes (12,288 cores) of a Cray XC30 supercomputer.
引用
收藏
页码:248 / 256
页数:9
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