桑格测序
大规模并行测序
破译
个人基因组学
计算生物学
人类基因组
癌症基因组测序
基因组
深度测序
霰弹枪测序
DNA测序
全基因组测序
单细胞测序
基因组学
计算机科学
外显子组测序
遗传学
生物
参考基因组
DNA
基因
突变
作者
Sam Behjati,Patrick Tarpey
标识
DOI:10.1136/archdischild-2013-304340
摘要
Next generation sequencing (NGS), massively parallel or deep sequencing are related terms that describe a DNA sequencing technology which has revolutionised genomic research. Using NGS an entire human genome can be sequenced within a single day. In contrast, the previous Sanger sequencing technology, used to decipher the human genome, required over a decade to deliver the final draft. Although in genome research NGS has mostly superseded conventional Sanger sequencing, it has not yet translated into routine clinical practice. The aim of this article is to review the potential applications of NGS in paediatrics.
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