分子遗传诊断技术综述

Rashmi S. Goswami, Shuko Harada
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引用次数: 5

摘要

自从人类基因组测序完成和许多检测遗传变异的技术发展以来,我们对遗传疾病的理解呈指数级增长。这些技术不仅使我们能够诊断遗传疾病,而且在这样做的过程中,还提供了对这些疾病发病机制的更多了解,以帮助开发适当的治疗方案。此外,下一代或大规模平行测序(NGS/MPS)的出现越来越多地用于临床环境,因为它可以检测从点突变到染色体重排以及转录组内的畸变等许多异常。在本文中,我们将讨论在遗传诊断中使用的多种技术。©2020 by John Wiley &儿子,Inc。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
An Overview of Molecular Genetic Diagnosis Techniques

Our understanding of genetic disease(s) has increased exponentially since the completion of human genome sequencing and the development of numerous techniques to detect genetic variants. These techniques have not only allowed us to diagnose genetic disease, but in so doing, also provide increased understanding of the pathogenesis of these diseases to aid in developing appropriate therapeutic options. Additionally, the advent of next-generation or massively parallel sequencing (NGS/MPS) is increasingly being used in the clinical setting, as it can detect a number of abnormalities from point mutations to chromosomal rearrangements as well as aberrations within the transcriptome. In this article, we will discuss the use of multiple techniques that are used in genetic diagnosis. © 2020 by John Wiley & Sons, Inc.

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来源期刊
Current Protocols in Human Genetics
Current Protocols in Human Genetics Biochemistry, Genetics and Molecular Biology-Genetics
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期刊介绍: Current Protocols in Human Genetics is the resource for designing and running successful research projects in all branches of human genetics.
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