Department of Bioengineering and Therapeutic Sciences, University of California San Francisco, San Francisco, California 94158, United States.
California Institute for Quantitative Biosciences, University of California San Francisco, San Francisco, California 94158, United States.
Anal Chem. 2021 May 25;93(20):7422-7429. doi: 10.1021/acs.analchem.0c04749. Epub 2021 May 10.
Targeted sequencing enables sensitive and cost-effective analysis by focusing resources on molecules of interest. Existing methods, however, are limited in enrichment power and target capture length. Here, we present a novel method that uses compound nucleic acid cytometry to achieve million-fold enrichments of molecules >10 kbp in length using minimal prior target information. We demonstrate the approach by sequencing HIV proviruses in infected individuals. Our method is useful for rare target sequencing in research and clinical applications, including for identifying cancer-associated mutations or sequencing viruses infecting cells.
靶向测序通过将资源集中在感兴趣的分子上,实现了灵敏且具有成本效益的分析。然而,现有的方法在富集能力和目标捕获长度上存在限制。在这里,我们提出了一种新的方法,该方法使用复合核酸细胞术,在最小的先验目标信息下,实现了长度大于 10 kbp 的分子的百万倍富集。我们通过对感染个体中的 HIV 前病毒进行测序来证明该方法的有效性。我们的方法可用于研究和临床应用中的稀有靶标测序,包括鉴定与癌症相关的突变或测序感染细胞的病毒。