Tolle Fabian, Mayer Günter
Life & Medical Sciences Institute (LIMES), University of Bonn, Gerhard-Domagk-Str. 1, Bonn, 53121, Germany.
Methods Mol Biol. 2016;1380:77-84. doi: 10.1007/978-1-4939-3197-2_6.
Fuelled by massive whole genome sequencing projects such as the human genome project, enormous technological advancements and therefore tremendous price drops could be achieved, rendering next-generation sequencing very attractive for deep sequencing of SELEX libraries. Herein we describe the preparation of SELEX samples for Illumina sequencing, based on the already established whole genome sequencing workflow. We describe the addition of barcode sequences for multiplexing and the adapter ligation, avoiding associated pitfalls.
在人类基因组计划等大规模全基因组测序项目的推动下,实现了巨大的技术进步,进而带来了价格的大幅下降,这使得下一代测序对于SELEX文库的深度测序极具吸引力。在此,我们基于已确立的全基因组测序工作流程,描述用于Illumina测序的SELEX样本的制备方法。我们还描述了用于多重分析的条形码序列的添加以及接头连接过程,并避免相关的陷阱。