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本文引用的文献

1
FastANOVA: an Efficient Algorithm for Genome-Wide Association Study.快速方差分析:一种用于全基因组关联研究的高效算法。
KDD. 2008:821-829.
2
Inferring missing genotypes in large SNP panels using fast nearest-neighbor searches over sliding windows.通过在滑动窗口上进行快速最近邻搜索来推断大型单核苷酸多态性(SNP)面板中缺失的基因型。
Bioinformatics. 2007 Jul 1;23(13):i401-7. doi: 10.1093/bioinformatics/btm220.
3
Two-stage two-locus models in genome-wide association.全基因组关联研究中的两阶段双基因座模型
PLoS Genet. 2006 Sep 22;2(9):e157. doi: 10.1371/journal.pgen.0020157.
4
A common genetic variant is associated with adult and childhood obesity.一种常见的基因变异与成人和儿童肥胖有关。
Science. 2006 Apr 14;312(5771):279-83. doi: 10.1126/science.1124779.
5
Comparison of type I error for multiple test corrections in large single-nucleotide polymorphism studies using principal components versus haplotype blocking algorithms.基于主成分分析和单倍型分组算法在大规模单核苷酸多态性研究中多重检验校正的Ⅰ类错误比较。
BMC Genet. 2005 Dec 30;6 Suppl 1(Suppl 1):S78. doi: 10.1186/1471-2156-6-S1-S78.
6
Genetic variation in laboratory mice.实验小鼠的基因变异
Nat Genet. 2005 Nov;37(11):1175-80. doi: 10.1038/ng1666.
7
Multiple locus linkage analysis of genomewide expression in yeast.酵母全基因组表达的多位点连锁分析
PLoS Biol. 2005 Aug;3(8):e267. doi: 10.1371/journal.pbio.0030267. Epub 2005 Jul 26.
8
Tag SNP selection in genotype data for maximizing SNP prediction accuracy.在基因型数据中选择标签单核苷酸多态性以最大化单核苷酸多态性预测准确性。
Bioinformatics. 2005 Jun;21 Suppl 1:i195-203. doi: 10.1093/bioinformatics/bti1021.
9
Modular epistasis in yeast metabolism.酵母代谢中的模块化上位性
Nat Genet. 2005 Jan;37(1):77-83. doi: 10.1038/ng1489. Epub 2004 Dec 12.
10
Mapping complex disease loci in whole-genome association studies.全基因组关联研究中的复杂疾病基因座定位
Nature. 2004 May 27;429(6990):446-52. doi: 10.1038/nature02623.

FastChi:一种用于分析基因-基因相互作用的高效算法。

FastChi: an efficient algorithm for analyzing gene-gene interactions.

作者信息

Zhang Xiang, Zou Fei, Wang Wei

机构信息

Department of Computer Science, University of North Carolina at Chapel Hill, USA.

出版信息

Pac Symp Biocomput. 2009:528-39.

PMID:19209728
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2728448/
Abstract

Recent advances in high-throughput genotyping have inspired increasing research interests in genome-wide association study for diseases. To understand underlying biological mechanisms of many diseases, we need to consider simultaneously the genetic effects across multiple loci. The large number of SNPs often makes multilocus association study very computationally challenging because it needs to explicitly enumerate all possible SNP combinations at the genome-wide scale. Moreover, with the large number of SNPs correlated, permutation procedure is often needed for properly controlling family-wise error rates. This makes the problem even more computationally demanding, since the test procedure needs to be repeated for each permuted data. In this paper, we present FastChi, an exhaustive yet efficient algorithm for genome-wide two-locus chi-square test. FastChi utilizes an upper bound of the two-locus chi-square test, which can be expressed as the sum of two terms--both are efficient to compute: the first term is based on the single-locus chi-square test for the given phenotype; and the second term only depends on the genotypes and is independent of the phenotype. This upper bound enables the algorithm to only perform the two-locus chi-square test on a small number of candidate SNP pairs without the risk of missing any significant ones. Since the second part of the upper bound only needs to be precomputed once and stored for subsequence uses, the advantage is more prominent in large permutation tests. Extensive experimental results demonstrate that our method is an order of magnitude faster than the brute force alternative.

摘要

高通量基因分型技术的最新进展激发了人们对疾病全基因组关联研究的浓厚兴趣。为了理解多种疾病的潜在生物学机制,我们需要同时考虑多个位点的遗传效应。大量的单核苷酸多态性(SNP)常常使得多位点关联研究在计算上极具挑战性,因为它需要在全基因组范围内明确枚举所有可能的SNP组合。此外,由于大量SNP之间存在相关性,通常需要采用置换程序来适当控制家族性错误率。这使得问题在计算上的要求更高,因为测试程序需要对每个置换后的数据重复进行。在本文中,我们提出了FastChi,一种用于全基因组两位点卡方检验的详尽而高效的算法。FastChi利用了两位点卡方检验的一个上界,该上界可以表示为两个项的和——这两个项都易于计算:第一项基于给定表型的单位点卡方检验;第二项仅取决于基因型,与表型无关。这个上界使得该算法只需对少量候选SNP对进行两位点卡方检验,而不会有遗漏任何显著SNP对的风险。由于上界的第二部分只需要预先计算一次并存储以供后续使用,在大型置换检验中这种优势更为突出。大量实验结果表明,我们的方法比暴力方法快一个数量级。