Gene mapping the world of complex diseases

Jörg Hager
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引用次数: 0

Abstract

Complex diseases such as obesity affect millions of people worldwide and yet the therapeutic options available to tackle their causes are limited. Identifying new drug targets by mapping disease-associated genes is made difficult by the fact that more than one gene might act synergistically to cause the condition. Many existing techniques rely on time-consuming characterisation of multiple genetic markers. A new approach, genome hybrid identity profiling, identifies DNA regions that are ‘identical by descent’ for the entire genomes of two related individuals. Isolating disease-associated genes in this way gives researchers a fast, precise way of identifying potential drug targets for treatment of complex diseases.

基因绘制复杂疾病的世界
肥胖等复杂疾病影响着全世界数百万人,但可用于解决其病因的治疗选择有限。通过绘制疾病相关基因图谱来确定新的药物靶点变得困难,因为多个基因可能协同作用导致疾病。许多现有的技术依赖于耗时的多个遗传标记的表征。一种新的方法,基因组杂交身份分析,确定了两个相关个体的整个基因组中“血统相同”的DNA区域。以这种方式分离疾病相关基因,为研究人员提供了一种快速、精确地识别治疗复杂疾病的潜在药物靶点的方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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