Library construction for next-generation sequencing: Overviews and challenges

被引:390
作者
Head, Steven R. [1 ]
Komori, H. Kiyomi [2 ]
LaMere, Sarah A. [2 ]
Whisenant, Thomas [2 ]
Van Nieuwerburgh, Filip [3 ]
Salomon, Daniel R. [2 ]
Ordoukhanian, Phillip [1 ]
机构
[1] Scripps Res Inst, NGS & Microarray Core Facil, La Jolla, CA 92037 USA
[2] Scripps Res Inst, Dept Mol & Expt Med, La Jolla, CA 92037 USA
[3] Univ Ghent, Fac Pharmaceut Sci, Lab Pharmaceut Biotechnol, B-9000 Ghent, Belgium
关键词
deep sequencing; DNA; RNA; library preparation; next-generation sequencing; RNA-seq; DNA-seq; ChIP-seq; RIP-seq; MESSENGER-RNA-SEQ; DNA METHYLATION; WIDE IDENTIFICATION; ANALYSIS REVEALS; GENE-EXPRESSION; CHIP-SEQ; IN-VIVO; GENOME; AMPLIFICATION; PROTEIN;
D O I
10.2144/000114133
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
High-throughput sequencing, also known as next-generation sequencing (NGS), has revolutionized genomic research. In recent years, NGS technology has steadily improved, with costs dropping and the number and range of sequencing applications increasing exponentially. Here, we examine the critical role of sequencing library quality and consider important challenges when preparing NGS libraries from DNA and RNA sources. Factors such as the quantity and physical characteristics of the RNA or DNA source material as well as the desired application (i.e., genome sequencing, targeted sequencing, RNA-seq, ChIP-seq, RIP-seq, and methylation) are addressed in the context of preparing high quality sequencing libraries. In addition, the current methods for preparing NGS libraries from single cells are also discussed.
引用
收藏
页码:61 / +
页数:13
相关论文
共 118 条
[1]   Rapid, low-input, low-bias construction of shotgun fragment libraries by high-density in vitro transposition [J].
Adey, Andrew ;
Morrison, Hilary G. ;
Asan ;
Xun, Xu ;
Kitzman, Jacob O. ;
Turner, Emily H. ;
Stackhouse, Bethany ;
MacKenzie, Alexandra P. ;
Caruccio, Nicholas C. ;
Zhang, Xiuqing ;
Shendure, Jay .
GENOME BIOLOGY, 2010, 11 (12)
[2]   Whole-genome chromatin profiling from limited numbers of cells using nano-ChIP-seq [J].
Adli, Mazhar ;
Bernstein, Bradley E. .
NATURE PROTOCOLS, 2011, 6 (10) :1656-1668
[3]   Analyzing and minimizing PCR amplification bias in Illumina sequencing libraries [J].
Aird, Daniel ;
Ross, Michael G. ;
Chen, Wei-Sheng ;
Danielsson, Maxwell ;
Fennell, Timothy ;
Russ, Carsten ;
Jaffe, David B. ;
Nusbaum, Chad ;
Gnirke, Andreas .
GENOME BIOLOGY, 2011, 12 (02)
[4]  
Armour CD, 2009, NAT METHODS, V6, P647, DOI [10.1038/NMETH.1360, 10.1038/nmeth.1360]
[5]   Technical Variations in Low-Input RNA-seq Methodologies [J].
Bhargava, Vipul ;
Head, Steven R. ;
Ordoukhanian, Phillip ;
Mercola, Mark ;
Subramaniam, Shankar .
SCIENTIFIC REPORTS, 2014, 4
[6]   Quantitative Transcriptomics using Designed Primer-based Amplification [J].
Bhargava, Vipul ;
Ko, Pang ;
Willems, Erik ;
Mercola, Mark ;
Subramaniam, Shankar .
SCIENTIFIC REPORTS, 2013, 3
[7]   Quantitative Sequencing of 5-Methylcytosine and 5-Hydroxymethylcytosine at Single-Base Resolution [J].
Booth, Michael J. ;
Branco, Miguel R. ;
Ficz, Gabriella ;
Oxley, David ;
Krueger, Felix ;
Reik, Wolf ;
Balasubramanian, Shankar .
SCIENCE, 2012, 336 (6083) :934-937
[8]   New methods for next generation sequencing based microRNA expression profiling [J].
Buermans, Henk P. J. ;
Ariyurek, Yavuz ;
van Ommen, Gertjan ;
den Dunnen, Johan T. ;
't Hoen, Peter A. C. .
BMC GENOMICS, 2010, 11
[9]   Protein families and RNA recognition [J].
Chen, Y ;
Varani, G .
FEBS JOURNAL, 2005, 272 (09) :2088-2097
[10]   Ectopic B-cell clusters that infiltrate transplanted human kidneys are clonal [J].
Cheng, Julong ;
Torkamani, Ali ;
Grover, Rajesh K. ;
Jones, Teresa M. ;
Ruiz, Diana I. ;
Schork, Nicholas J. ;
Quigley, Michael M. ;
Hall, F. Wesley ;
Salomon, Daniel R. ;
Lerner, Richard A. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2011, 108 (14) :5560-5565