Atlas-scale single-cell DNA methylation profiling with sciMETv3.

IF 11.1 Q1 CELL BIOLOGY
Cell genomics Pub Date : 2025-01-08 Epub Date: 2024-12-23 DOI:10.1016/j.xgen.2024.100726
Ruth V Nichols, Lauren E Rylaarsdam, Brendan L O'Connell, Zohar Shipony, Nika Iremadze, Sonia N Acharya, Andrew C Adey
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引用次数: 0

Abstract

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.

使用sciMETv3进行atlas级单细胞DNA甲基化分析。
与其他方法相比,评估DNA甲基化的单细胞方法在每次实验中没有达到相同的细胞通量水平,大规模数据集需要广泛的自动化、时间和其他资源。在这里,我们描述了sciMETv3,这是一种基于组合索引的技术,可以在单个实验中生成地图集规模的库。为了减少测序负担,我们展示了sciMETv3与捕获技术的兼容性,以丰富调控区域,以及利用酶转化的能力,这可以产生更高的文库多样性。我们通过使用Illumina和Ultima测序仪器从四个多路个体中分离的人类额叶中回中产生bb10140,000个细胞文库来展示sciMETv3的吞吐量。最后,我们引入sciMET+ATAC来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。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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CiteScore
7.10
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