基因绘制复杂疾病的世界

Jörg Hager
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引用次数: 0

摘要

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。
Gene mapping the world of complex diseases

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.

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