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A Haplotype Based Method for Genetic Disease Susceptibility Prediction

机译:一种基于单倍型的遗传疾病易感性预测方法

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摘要

High-throughput single nucleotide polymorphism (SNP) genotyping technologies make massive genotype data, with a large number of individuals, publicly available. Accessibility of genetic data makes genome-wide association studies for complex diseases possible. The susceptibility to complex diseases can be predicted through the analysis of the genetic data and prospective patients can be helped to make informed decisions. With the development of DNA microarray technique, it is possible to access the human genetic information related to specific diseases, but most disease association studies are based on genotypes. This paper uses a combinatorial method to analyze the haplotype data for Crohn's disease and search disease-associated factors for given case/control samples. A Linear programming based method has been applied to publicly available genotype data on Crohn's disease for association study and achieved a promising result.
机译:高通量单核苷酸多态性(SNP)基因分型技术使巨大的基因型数据具有大量的个人,公开可用。遗传数据的可访问性使得全基因组关联研究成为复杂疾病。通过对遗传数据的分析,可以通过分析来预测对复杂疾病的敏感性,并且可以帮助提出明智的决定。随着DNA微阵列技术的发展,可以访问与特定疾病相关的人类遗传信息,但大多数疾病协会研究都是基于基因型。本文采用组​​合方法来分析克罗恩病的单倍型数据,以及给定案例/对照样品的搜索疾病相关因素。基于线性规划的方法已应用于Crohn病症的公开可用的基因型数据进行关联研究,并实现了有希望的结果。

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