Cancer Institute NSW EC Fellow, University of Newcastle
Friday 22nd March
Agar Theatre, BioSciences 4 Building, The University of Melbourne
Single Cell Epigenomics for Analysis of Rare and Heterogeneous Cell Populations
Single-cell sequencing technologies are revolutionising our understanding of heterogeneous cell populations in development and disease. Incorporation of epigenetic information with single-cell transcriptomic and genomic analyses will provide valuable insights into the molecular mechanisms of gene regulation (1). DNA methylation occurs on cytosine residues of CpG dinucleotides in mammalian cells. This epigenetic modification is dynamically regulated during development and is globally dysregulated in many cancer types. We developed single-cell bisulphite sequencing (scBS-seq) (2), which provides quantitative, single-nucleotide information on DNA methylation for up to 50% of cytosines across the genome. Extending on this work, we reported parallel single-cell methylome and transcriptome sequencing (scM&T-seq) (3), which allows both DNA methylation and gene expression to be assayed from the same single cell. To illustrate the power of integrated single-cell multi-omics, biological insights gained from scM&T-seq analysis of mouse embryonic stem cells will be presented. Ongoing technological developments will also be described.
1. Clark, Lee, Smallwood et al. (2016) Genome Biol 17:72.
2. Smallwood, Lee, et al. (2014) Nat Methods 11:817-20.
3. Angermueller, Clark, Lee, Macaulay, et al. (2016) Nat Methods 13:229-32.
Enquiries: Andrew Siebel (firstname.lastname@example.org)