Australian Institute of Bioengineering and Nanotechnology, University of Queensland, Brisbane, QLD, Australia.
Kinghorn Centre for Clinical Genomics, Garvan Institute of Medical Research, Sydney, NSW, Australia.
Nat Commun. 2022 Oct 28;13(1):6437. doi: 10.1038/s41467-022-34028-8.
Library adaptors are short oligonucleotides that are attached to RNA and DNA samples in preparation for next-generation sequencing (NGS). Adaptors can also include additional functional elements, such as sample indexes and unique molecular identifiers, to improve library analysis. Here, we describe Control Library Adaptors, termed CAPTORs, that measure the accuracy and reliability of NGS. CAPTORs can be integrated within the library preparation of RNA and DNA samples, and their encoded information is retrieved during sequencing. We show how CAPTORs can measure the accuracy of nanopore sequencing, evaluate the quantitative performance of metagenomic and RNA sequencing, and improve normalisation between samples. CAPTORs can also be customised for clinical diagnoses, correcting systematic sequencing errors and improving the diagnosis of pathogenic BRCA1/2 variants in breast cancer. CAPTORs are a simple and effective method to increase the accuracy and reliability of NGS, enabling comparisons between samples, reagents and laboratories, and supporting the use of nanopore sequencing for clinical diagnosis.
文库接头是短的寡核苷酸,在进行下一代测序(NGS)之前连接到 RNA 和 DNA 样本上。接头还可以包括其他功能元件,如样本索引和独特的分子标识符,以改善文库分析。在这里,我们描述了控制文库接头,称为 CAPTORs,它们可以测量 NGS 的准确性和可靠性。CAPTORs 可以整合在 RNA 和 DNA 样本的文库制备过程中,并在测序过程中检索其编码信息。我们展示了 CAPTORs 如何测量纳米孔测序的准确性,评估宏基因组和 RNA 测序的定量性能,并改善样本之间的归一化。CAPTORs 还可以针对临床诊断进行定制,纠正系统测序错误,并改善乳腺癌中致病性 BRCA1/2 变体的诊断。CAPTORs 是一种简单有效的方法,可以提高 NGS 的准确性和可靠性,实现样本、试剂和实验室之间的比较,并支持纳米孔测序用于临床诊断。