Nichols Ruth V, Rylaarsdam Lauren E, O'Connell Brendan L, Shipony Zohar, Iremadze Nika, Acharya Sonia N, Adey Andrew C
Department of Molecular & Medical Genetics, Oregon Health & Science University, Portland, OR, USA.
Department of Molecular & Medical Genetics, Oregon Health & Science University, Portland, OR, USA; Cancer Early Detection Advanced Research Institute, Oregon Health & Science University, Portland, OR, USA.
Cell Genom. 2025 Jan 8;5(1):100726. doi: 10.1016/j.xgen.2024.100726. Epub 2024 Dec 23.
Single-cell methods to assess DNA methylation have not achieved the same level of cell throughput per experiment compared to other modalities, with large-scale datasets requiring extensive automation, time, and other resources. Here, we describe sciMETv3, a combinatorial indexing-based technique that enables atlas-scale libraries to be produced in a single experiment. To reduce the sequencing burden, we demonstrate the compatibility of sciMETv3 with capture techniques to enrich regulatory regions, as well as the ability to leverage enzymatic conversion, which can yield higher library diversity. We showcase the throughput of sciMETv3 by producing a >140,000 cell library from human middle frontal gyrus split across four multiplexed individuals using both Illumina and Ultima sequencing instrumentation. Finally, we introduce sciMET+ATAC to enable high-throughput exploration of the interplay between chromatin accessibility and DNA methylation within the same cell.
与其他方法相比,用于评估DNA甲基化的单细胞方法在每次实验中尚未达到相同水平的细胞通量,大规模数据集需要大量的自动化操作、时间和其他资源。在此,我们描述了sciMETv3,这是一种基于组合索引的技术,能够在单个实验中生成图谱规模的文库。为了减轻测序负担,我们证明了sciMETv3与捕获技术的兼容性,以富集调控区域,以及利用酶促转化的能力,这可以产生更高的文库多样性。我们通过使用Illumina和Ultima测序仪器从四个多重个体的人类额中回产生一个超过140,000个细胞的文库,展示了sciMETv3的通量。最后,我们引入了sciMET+ATAC,以实现对同一细胞内染色质可及性和DNA甲基化之间相互作用的高通量探索。