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通过粒子群优化生成单核苷酸多态性(SNP)条形码以评估疾病的SNP-SNP相互作用。

Generating SNP barcode to evaluate SNP-SNP interaction of disease by particle swarm optimization.

作者信息

Chang Hsueh-Wei, Yang Cheng-Hong, Ho Chang-Hsuan, Wen Cheng-Hao, Chuang Li-Yeh

机构信息

Faculty of Biomedical Science and Environmental Biology, Kaohsiung Medical University, Kaohsiung, Taiwan.

出版信息

Comput Biol Chem. 2009 Feb;33(1):114-9. doi: 10.1016/j.compbiolchem.2008.07.029. Epub 2008 Aug 8.

Abstract

Genome-wide association analysis involved many single-nucleotide polymorphisms (SNPs) data is challenging mathematically and computationally. Hence, we propose the odds ratio-based discrete binary particle swarm optimization (OR-DBPSO) method that uses the OR as a new quantitative measure of disease risk among many SNP combinations with genotypes called "SNP barcode". DBPSO are applied to generate SNP barcode, which computes the maximal difference of occurrence between the case and control groups, to predict disease susceptibility such as osteoporosis. Different SNP barcode patterns may occur several times in either low or high bone mineral density (BMD) groups. Our results showed that a DBPSO can effectively identify a specific SNP barcode with an optimized fitness value. SNP barcodes with a low fitness value will naturally be discarded from the population. A representative SNP barcode with a variable number of SNPs is processed to OR analysis to determine the maximum difference between the low and high BMD groups in statistics manner. Therefore, this paper introduces a powerful procedure to analyze disease-associated SNP-SNP interaction in genome-wide genes.

摘要

涉及许多单核苷酸多态性(SNP)数据的全基因组关联分析在数学和计算方面都具有挑战性。因此,我们提出了基于比值比的离散二进制粒子群优化(OR-DBPSO)方法,该方法使用比值比作为一种新的疾病风险定量测量方法,用于在许多具有称为“SNP条形码”的基因型的SNP组合中。应用DBPSO生成SNP条形码,其计算病例组和对照组之间出现的最大差异,以预测骨质疏松症等疾病易感性。不同的SNP条形码模式可能在低骨密度或高骨密度(BMD)组中出现多次。我们的结果表明,DBPSO可以有效地识别具有优化适应度值的特定SNP条形码。适应度值低的SNP条形码将自然地从群体中丢弃。对具有可变数量SNP的代表性SNP条形码进行比值比分析,以统计学方式确定低BMD组和高BMD组之间的最大差异。因此,本文介绍了一种强大的程序来分析全基因组基因中与疾病相关的SNP-SNP相互作用。

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