Wong Koon Ho, Jin Yi, Moqtaderi Zarmik
Harvard Medical School, Boston, Massachusetts, USA.
Curr Protoc Mol Biol. 2013;Chapter 7:Unit 7.11.. doi: 10.1002/0471142727.mb0711s101.
The amount of sequence obtained by modern sequencing machines greatly exceeds the sequencing depth requirements of many experiments, especially those involving organisms with small genomes. In the interest of economy and efficiency, various strategies have been developed for multiplexing, in which samples are uniquely tagged with short identifying sequences known as barcodes, pooled, and then sequenced together in a single lane. The resulting combined sequence data are subsequently sorted by barcode before bioinformatic analysis. This unit contains a barcoding protocol for the preparation of up to 96 ChIP samples for multiplex sequencing in a single flow cell lane on the Illumina platform. This strategy may be extended to even larger numbers of samples and may also be generalized to other sequencing applications or sequencing platforms.
现代测序仪获得的序列数量远远超过许多实验的测序深度要求,特别是那些涉及小基因组生物的实验。出于经济和效率的考虑,已经开发了各种多重化策略,其中样本用称为条形码的短识别序列进行唯一标记,汇集在一起,然后在单个泳道中一起测序。随后,在进行生物信息分析之前,根据条形码对得到的组合序列数据进行分类。本单元包含一种条形码方案,用于在Illumina平台的单个流动池泳道中制备多达96个用于多重测序的ChIP样本。这种策略可以扩展到更多数量的样本,也可以推广到其他测序应用或测序平台。