TY - JOUR
T1 - Chromatin as self-returning walks
T2 - From population to single cell and back
AU - Shim, Anne R.
AU - Huang, Kai
AU - Backman, Vadim
AU - Szleifer, Igal
N1 - Publisher Copyright:
© 2021 The Authors
PY - 2022/3/9
Y1 - 2022/3/9
N2 - With a growing understanding of the chromatin structure, many efforts remain focused on bridging the gap between what is suggested by population-averaged data and what is visualized for single cells. A popular approach to traversing these scales is to fit a polymer model to Hi-C contact data. However, Hi-C is an average of millions to billions of cells, and each cell may not contain all population-averaged contacts. Therefore, we employ a novel approach of summing individual chromosome trajectories—determined by our Self-Returning Random Walk model—to create populations of cells. We allow single cells to consist of disparate structures and reproduce a variety of experimentally relevant contact maps. We show that the amount of shared topology between cells, and their mechanism of formation, changes the population-averaged structure. Therefore, we present a modeling technique that, with few constraints and little oversight, can be used to understand which single-cell chromatin structures underlie population-averaged behavior.
AB - With a growing understanding of the chromatin structure, many efforts remain focused on bridging the gap between what is suggested by population-averaged data and what is visualized for single cells. A popular approach to traversing these scales is to fit a polymer model to Hi-C contact data. However, Hi-C is an average of millions to billions of cells, and each cell may not contain all population-averaged contacts. Therefore, we employ a novel approach of summing individual chromosome trajectories—determined by our Self-Returning Random Walk model—to create populations of cells. We allow single cells to consist of disparate structures and reproduce a variety of experimentally relevant contact maps. We show that the amount of shared topology between cells, and their mechanism of formation, changes the population-averaged structure. Therefore, we present a modeling technique that, with few constraints and little oversight, can be used to understand which single-cell chromatin structures underlie population-averaged behavior.
UR - http://www.scopus.com/inward/record.url?scp=85133689119&partnerID=8YFLogxK
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U2 - 10.1016/j.bpr.2021.100042
DO - 10.1016/j.bpr.2021.100042
M3 - Short survey
C2 - 36425085
AN - SCOPUS:85133689119
SN - 2667-0747
VL - 2
JO - Biophysical Reports
JF - Biophysical Reports
IS - 1
M1 - 100042
ER -