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GWISFI: A universal GPU interface for exhaustive search of pairwise interactions in case-control GWAS in minutes

机译:GWIS FI :通用GPU接口,可在几分钟之内彻底搜索案例控制GWAS中的成对交互

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Epistatic interactions between genes are believed to be a critical component in the genetic architecture of complex diseases. Genome Wide Association Studies (GWAS) may be able to detect such genetic interactions indirectly, via the identification of associated SNP markers. Major obstacles to progress in this area are: the unknown nature of epistatic interactions, little understanding of the capabilities of different filtering methods, and the computational difficulties for exhaustive analysis. A common platform enabling various detection methods is needed to avoid practical issues such as software compatibility and portability, incompatible input and output formats and varying demands on computational resources. We developed a highly optimised GPU system capable of exhaustively analysing all SNP-pairs in typical GWAS data (0.5M SNPs, 5K samples) in a few minutes on a standard desktop computer. A number of programming elements provided by a functional interface can be used to construct user-defined statistical tests to efficiently score every SNP pair. As a proof of principle, we have implemented 8 methods from the literature via our interface. We have applied all of them using a single GPU to exhaustively scan the 7 popular WTCCC case-control GWAS datasets. We present timing results for these methods, both in their original software implementations and using our platform. Significant improvements in timing are observed, up to 10000 times for CPU implementations of the popular FastEpistasis in PLINK and up to 2 orders of magnitude for some GPU implementations in the literature. As an initial discovery we show plots for overlaps of list of selected pairs by 8 algorithms for Type 2 Diabetes, WTCCC data.
机译:基因之间的上位相互作用被认为是复杂疾病的遗传结构中的关键组成部分。基因组广泛关联研究(GWAS)可能能够通过鉴定相关的SNP标记间接检测这种遗传相互作用。在这一领域取得进展的主要障碍是:上位相互作用的未知性质,对不同过滤方法的功能了解甚少以及详尽分析的计算难度。为了避免实际问题,例如软件兼容性和可移植性,不兼容的输入和输出格式以及对计算资源的需求变化,需要一个启用各种检测方法的通用平台。我们开发了高度优化的GPU系统,能够在标准台式计算机上在几分钟内详尽分析典型GWAS数据(0.5M SNP,5K样本)中的所有SNP对。功能接口提供的许多编程元素可用于构建用户定义的统计测试,以有效地对每个SNP对进行评分。作为原理的证明,我们已经通过界面实现了文献中的8种方法。我们已经使用单个GPU应用了所有这些对象,以详尽地扫描7种流行的WTCCC案例控制GWAS数据集。我们在这些方法的原始软件实现中以及使用我们的平台时均会给出计时结果。观察到时序方面的显着改善,在文献中,PLINK中流行的FastEpistasis的CPU实现达到10000倍,某些GPU实现达到2个数量级。作为最初的发现,我们通过8种2型糖尿病,WTCCC数据算法显示了选定对列表重叠的图。

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