Bronner Iraad F, Quail Michael A
Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridgeshire, United Kingdom.
Curr Protoc Hum Genet. 2019 Jun;102(1):e86. doi: 10.1002/cphg.86.
In this unit, we describe a set of protocols and recommendations for Illumina library preparation. We review best practices in template quantitation methods; template fragmentation methodologies; solid-phase reverse-immobilization cleanup, including buffer exchange and size selection; end repair, A-tailing, and adapter ligation; indexing strategies; considerations regarding whether to use polymerase chain reaction; final library quantification methodologies; and normalization and pooling strategies. These workflows are applicable to both high-throughput and low-throughput Illumina library preparation and should help reduce bias, increase cost effectiveness, and produce high library yields. This is an extensive update of the previous version of this unit. © 2019 by John Wiley & Sons, Inc.
在本单元中,我们描述了一套用于Illumina文库制备的方案和建议。我们回顾了模板定量方法、模板片段化方法、固相反向固定化纯化(包括缓冲液交换和大小选择)、末端修复、A加尾和接头连接、索引策略、关于是否使用聚合酶链反应的考虑因素、最终文库定量方法以及标准化和混合策略等方面的最佳实践。这些工作流程适用于高通量和低通量Illumina文库制备,应有助于减少偏差、提高成本效益并产生高文库产量。这是本单元上一版本的全面更新。© 2019约翰威立国际出版公司。