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摘要

本章重点介绍人类基因组计划(HGP),该计划确定人类有20,000至25,000个蛋白质编码基因,只有约1.5%的基因组编码蛋白质,rRNA和tRNA。剩下的曾经被称为“垃圾DNA”的DNA,今天被认为对物种的生存至关重要。研究表明,基因不是连续的,有些基因发生在其他基因的内含子内;一些基因可以在相同或不同的DNA链上相互重叠,具有共享的编码和/或调节元件;此外,绝大多数人类基因都经历了选择性剪接,导致同一基因编码不同的蛋白质。基因组学和基因测序技术的进步为提供个性化医疗服务创造了难得的机会。临床基因检测有助于识别与许多疾病和健康状况风险相关的基因变异。
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Genomics and Genetic Testing
This chapter focuses on the Human Genome Project (HGP), which determined that humans have between 20,000 to 25,000 protein-coding genes and only about 1.5% of the genome codes for proteins, rRNA, and tRNA. The remainder once referred as “junk DNA” is today known to be crucial to survival of the species. Research indicates that genes are not contiguous, and some genes occur within the introns of other genes; some genes can overlap with each other either on the same or on different DNA strands with shared coding and/or regulatory elements; plus, the vast majority of human genes undergo alternative splicing leading to different proteins being encoded by the same gene. Advances in genomics and gene sequencing technologies have created exceptional opportunities for the delivery of personalized medical care. Clinical genetic testing has been helpful in identifying gene variants associated with risks for a number of diseases and health conditions.
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