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EMeth:一种基于 DNA 甲基化数据的细胞类型分解的 EM 算法。

EMeth: An EM algorithm for cell type decomposition based on DNA methylation data.

机构信息

Department of Statistics, University of Washington, Seattle, USA.

Department of Biostatistics, University of Washington, Seattle, USA.

出版信息

Sci Rep. 2021 Mar 11;11(1):5717. doi: 10.1038/s41598-021-84864-9.

Abstract

We introduce a new computational method named EMeth to estimate cell type proportions using DNA methylation data. EMeth is a reference-based method that requires cell type-specific DNA methylation data from relevant cell types. EMeth improves on the existing reference-based methods by detecting the CpGs whose DNA methylation are inconsistent with the deconvolution model and reducing their contributions to cell type decomposition. Another novel feature of EMeth is that it allows a cell type with known proportions but unknown reference and estimates its methylation. This is motivated by the case of studying methylation in tumor cells while bulk tumor samples include tumor cells as well as other cell types such as infiltrating immune cells, and tumor cell proportion can be estimated by copy number data. We demonstrate that EMeth delivers more accurate estimates of cell type proportions than several other methods using simulated data and in silico mixtures. Applications in cancer studies show that the proportions of T regulatory cells estimated by DNA methylation have expected associations with mutation load and survival time, while the estimates from gene expression miss such associations.

摘要

我们引入了一种新的计算方法,名为 EMeth,用于使用 DNA 甲基化数据估计细胞类型比例。EMeth 是一种基于参考的方法,需要来自相关细胞类型的特定于细胞类型的 DNA 甲基化数据。EMeth 通过检测与去卷积模型不一致的 CpG 并减少它们对细胞类型分解的贡献,改进了现有的基于参考的方法。EMeth 的另一个新颖特征是它允许具有已知比例但未知参考的细胞类型进行估计,并估计其甲基化。这是受到研究肿瘤细胞甲基化时的情况的启发,此时批量肿瘤样本包括肿瘤细胞以及其他细胞类型,如浸润免疫细胞,并且可以通过拷贝数数据估计肿瘤细胞比例。我们证明,使用模拟数据和模拟混合物,EMeth 比其他几种方法提供了更准确的细胞类型比例估计。在癌症研究中的应用表明,DNA 甲基化估计的 T 调节细胞比例与突变负荷和生存时间有预期的关联,而来自基因表达的估计则没有这种关联。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a0fd/7952399/417fc8400cad/41598_2021_84864_Fig1_HTML.jpg

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