Chapter 21
Single Cell Analysis and Multiomics
The assumption of average types is one of the major simplifying assumptions needed
to produce a mechanistic description of a natural system. 1 Besides, the limited sen-
sitivity of many experimental methods made it necessary to gather materials from
large numbers of cells in order to have a sufficient number of molecules for reli-
able characterization. Continual increases in sensitivity have now made it feasible
to analyse the genome, transcriptome, proteome, metabolome, and so forth from a
single cell, enabling individual heterogeneity even within a single tissue containing
only cells of the same type to be demonstrated.
One contribution to this heterogeneity, especially apparent in rapidly self-renewing
tissues such as the intestinal epithelium, blood, and skin, is the fact that development
of the final type from an undifferentiated stem cell is a continuum, and many interme-
diate types are likely to be found in such tissues. Understanding these development
trajectories is difficult or impossible if the attributes of cells of many different stages
are averaged out in the examination.
Even in a perfectly synchronized tissue, however, there is likely to be heterogeneity
because of the amplification up to macroscopic expression of microscopic, random
variations; they are countered by “peer pressure” (compeer coercion) tending to
produce uniformity.
Especially when working with the minute quantities of material available from a
single cell (e.g., total RNA may amount to some tens of picograms) close to or at
the limits of detection of the employed techniques, 2 it was natural to simultaneously
characterize many features to provide corroboration. Hence multiomics was born,
in which the genome, transcriptome, proteome, metabolome, etc., are characterized
and compared, an approach that may ultimately become routine for all biological
investigations.
1 Allen (2007).
2 See, e.g., Adil et al. (2021).
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