基因组测序在鉴定新的治疗靶点中的作用

K. Alharbi, I. Khan, Y. Tejaswini, Y. A. Devi
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引用次数: 4

摘要

近年来出现了显著的技术创新,使快速和具有成本效益的全基因组直接测序成为可能。这一代大量的基因组数据是基于这样的假设:对基因组学的更好理解将有助于确定遗传疾病的新原因,以及发现新的治疗靶点。由于这一假设,来自不同生物体(包括人类)的许多基因组已被测序,从而产生了大量的遗传数据。然而,为了最好地利用这些数据,我们处理和分析大规模数据的能力也有必要进行类似的扩展。本文综述了基因组测序项目对新基因和蛋白质鉴定的影响,特别关注了病原基因组测序在潜在药物开发中的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The Role of Genome Sequencing in the Identification of Novel Therapeutic Targets
Remarkable technological innovations have emerged in recent years allowing for rapid and cost-effective whole genome direct sequencing. This generation of massive amounts of genomic data was made with the assumption that the better understanding of the Genomics would aid in the identification of new causes for genetic disorders, as well as discovering new therapeutic targets. Due to this assumption, many genomes from different organisms, including humans, have been sequenced, resulting in an immense amount of genetic data. However, in order to best use this data, a similar expansion in our ability to process and analyze the data on a large scale will be necessary. The present review focuses on the impact of genome sequencing projects on the identification of novel genes and proteins, with a special focus on the role of sequencing pathogenic genomes in potential drug development.
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