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Understanding multicellular physiology and pathobiology requires analysis of the relationship between genotype, chromatin organisation and phenotype. In the multi-omics era, many methods exist to investigate biological processes across the genome, transcriptome, epigenome, proteome and metabolome. Until recently, this was only possible for populations of cells or complex tissues, creating an averaging effect that may obscure direct correlations between multiple layers of data. Single-cell sequencing methods have removed this averaging effect, but computational integration after profiling distinct modalities separately may still not completely reflect underlying biology. Multiplexed assays resolving multiple modalities in the same cell are required to overcome these shortcomings and have the potential to deliver unprecedented understanding of biology and disease.

Original publication

DOI

10.1016/j.cbpa.2020.01.013

Type

Journal article

Journal

Curr opin chem biol

Publication Date

15/04/2020

Volume

57

Pages

17 - 26

Keywords

Multiplexed single-cell assays, Next-generation sequencing, Single cell, Single-cell epigenomics