High-Throughput Sequencing Technologies

被引：843

作者：

Reuter, Jason A. ^{[1
]}

Spacek, Damek V. ^{[1
]}

Snyder, Michael P. ^{[1
]}

机构：

[1] Stanford Univ, Dept Genet, Sch Med, Stanford, CA 94305 USA

来源：

MOLECULAR CELL | 2015年 / 58卷 / 04期

关键词：

GENOME-WIDE IDENTIFICATION; RNA SECONDARY STRUCTURE; SINGLE-MOLECULE; DNA METHYLATION; IN-VIVO; STRUCTURAL VARIATION; CLONAL EVOLUTION; HIGH-RESOLUTION; NONCODING RNAS; GUT MICROBIOME;

D O I：

10.1016/j.molcel.2015.05.004

中图分类号：

Q5 [生物化学]; Q7 [分子生物学];

学科分类号：

071010 ; 081704 ;

摘要：

The human genome sequence has profoundly altered our understanding of biology, human diversity, and disease. The path from the first draft sequence to our nascent era of personal genomes and genomic medicine has been made possible only because of the extraordinary advancements in DNA sequencing technologies over the past 10 years. Here, we discuss commonly used high-throughput sequencing platforms, the growing array of sequencing assays developed around them, as well as the challenges facing current sequencing platforms and their clinical application.

引用

页码：586 / 597

页数：12

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