Virtual methylome dissection facilitated by single-cell analyses
| dc.contributor.author | Yin, Liduo | en |
| dc.contributor.author | Luo, Yanting | en |
| dc.contributor.author | Xu, Xiguang | en |
| dc.contributor.author | Wen, Shiyu | en |
| dc.contributor.author | Wu, Xiaowei | en |
| dc.contributor.author | Lu, Xuemei | en |
| dc.contributor.author | Xie, Hehuang David | en |
| dc.contributor.department | Biological Sciences | en |
| dc.contributor.department | Biomedical Sciences and Pathobiology | en |
| dc.contributor.department | Statistics | en |
| dc.contributor.department | Fralin Life Sciences Institute | en |
| dc.date.accessioned | 2019-11-18T13:03:08Z | en |
| dc.date.available | 2019-11-18T13:03:08Z | en |
| dc.date.issued | 2019-11-11 | en |
| dc.date.updated | 2019-11-17T04:20:17Z | en |
| dc.description.abstract | Background Numerous cell types can be identified within plant tissues and animal organs, and the epigenetic modifications underlying such enormous cellular heterogeneity are just beginning to be understood. It remains a challenge to infer cellular composition using DNA methylomes generated for mixed cell populations. Here, we propose a semi-reference-free procedure to perform virtual methylome dissection using the nonnegative matrix factorization (NMF) algorithm. Results In the pipeline that we implemented to predict cell-subtype percentages, putative cell-type-specific methylated (pCSM) loci were first determined according to their DNA methylation patterns in bulk methylomes and clustered into groups based on their correlations in methylation profiles. A representative set of pCSM loci was then chosen to decompose target methylomes into multiple latent DNA methylation components (LMCs). To test the performance of this pipeline, we made use of single-cell brain methylomes to create synthetic methylomes of known cell composition. Compared with highly variable CpG sites, pCSM loci achieved a higher prediction accuracy in the virtual methylome dissection of synthetic methylomes. In addition, pCSM loci were shown to be good predictors of the cell type of the sorted brain cells. The software package developed in this study is available in the GitHub repository (https://github.com/Gavin-Yinld). Conclusions We anticipate that the pipeline implemented in this study will be an innovative and valuable tool for the decoding of cellular heterogeneity. | en |
| dc.description.version | Published version | en |
| dc.format.mimetype | application/pdf | en |
| dc.identifier.citation | Epigenetics & Chromatin. 2019 Nov 11;12(1):66 | en |
| dc.identifier.doi | https://doi.org/10.1186/s13072-019-0310-9 | en |
| dc.identifier.uri | http://hdl.handle.net/10919/95565 | en |
| dc.language.iso | en | en |
| dc.rights | Creative Commons Attribution 4.0 International | en |
| dc.rights.holder | The Author(s) | en |
| dc.rights.uri | http://creativecommons.org/licenses/by/4.0/ | en |
| dc.title | Virtual methylome dissection facilitated by single-cell analyses | en |
| dc.title.serial | Epigenetics & Chromatin | en |
| dc.type | Article - Refereed | en |
| dc.type.dcmitype | Text | en |