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外显子组测序:全基因组测序前的甜蜜点。

Exome sequencing: the sweet spot before whole genomes.

机构信息

Genetic Disease Research Branch, National Human Genome Research Institute, National Institutes of Health, 5625 Fishers Lane, Bethesda, MD 20892, USA.

出版信息

Hum Mol Genet. 2010 Oct 15;19(R2):R145-51. doi: 10.1093/hmg/ddq333. Epub 2010 Aug 12.

Abstract

The development of massively parallel sequencing technologies, coupled with new massively parallel DNA enrichment technologies (genomic capture), has allowed the sequencing of targeted regions of the human genome in rapidly increasing numbers of samples. Genomic capture can target specific areas in the genome, including genes of interest and linkage regions, but this limits the study to what is already known. Exome capture allows an unbiased investigation of the complete protein-coding regions in the genome. Researchers can use exome capture to focus on a critical part of the human genome, allowing larger numbers of samples than are currently practical with whole-genome sequencing. In this review, we briefly describe some of the methodologies currently used for genomic and exome capture and highlight recent applications of this technology.

摘要

高通量测序技术的发展,加上新的高通量 DNA 富集技术(基因组捕获),使得在越来越多的样本中对人类基因组的靶向区域进行测序成为可能。基因组捕获可以靶向基因组中的特定区域,包括感兴趣的基因和连锁区域,但这限制了研究的范围,使其只能针对已知的内容。外显子组捕获允许对基因组中的完整蛋白编码区域进行无偏倚的研究。研究人员可以使用外显子组捕获来专注于人类基因组的关键部分,从而允许在当前全基因组测序可行的情况下增加更多的样本数量。在这篇综述中,我们简要描述了目前用于基因组和外显子组捕获的一些方法,并强调了该技术的最新应用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3b71/2953745/6e0c1df1f26d/ddq33301.jpg

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