We present Epiclomal, a probabilistic clustering method arising from a hierarchical mixture model to simultaneously cluster sparse single-cell DNA methylation data and impute missing values. Using synthetic and published single-cell CpG datasets, we show that Epiclomal outperforms non-probabilistic methods and can handle the inherent missing data characteristic that dominates single-cell CpG genome sequences. Using newly generated single-cell 5mCpG sequencing data, we show that Epiclomal discovers sub-clonal methylation patterns in aneuploid tumour genomes, thus defining epiclones that can match or transcend copy number-determined clonal lineages and opening up an important form of clonal analysis in cancer. Epiclomal is written in R and Python and is available at https://github.com/shahcompbio/Epiclomal.
CITATION STYLE
de Souza, C. P. E., Andronescu, M., Masud, T., Kabeer, F., Biele, J., Laks, E., … Shah, S. P. (2020). Epiclomal: Probabilistic clustering of sparse single-cell DNA methylation data. PLoS Computational Biology, 16(9). https://doi.org/10.1371/journal.pcbi.1008270
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