Research output: Contribution to journal › Review article › peer-review
Predicting Genome Architecture: Challenges and Solutions. / Belokopytova, Polina; Fishman, Veniamin.
In: Frontiers in Genetics, Vol. 11, 617202, 22.01.2021.Research output: Contribution to journal › Review article › peer-review
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TY - JOUR
T1 - Predicting Genome Architecture: Challenges and Solutions
AU - Belokopytova, Polina
AU - Fishman, Veniamin
N1 - Funding Information: We thank Emil Valeev and Olga Gladkih who helped us with designing illustrations. Funding. This work was supported by the RSF grant #19-74-00102. Computations have shown in Figure 3 were performed using nodes of the Novosibirsk State University high-throughput computation cluster [supported by the Ministry of Education and Science of Russian Federation, grant #2019-0546 (FSUS-2020-0040)].
PY - 2021/1/22
Y1 - 2021/1/22
N2 - Genome architecture plays a pivotal role in gene regulation. The use of high-throughput methods for chromatin profiling and 3-D interaction mapping provide rich experimental data sets describing genome organization and dynamics. These data challenge development of new models and algorithms connecting genome architecture with epigenetic marks. In this review, we describe how chromatin architecture could be reconstructed from epigenetic data using biophysical or statistical approaches. We discuss the applicability and limitations of these methods for understanding the mechanisms of chromatin organization. We also highlight the emergence of new predictive approaches for scoring effects of structural variations in human cells.
AB - Genome architecture plays a pivotal role in gene regulation. The use of high-throughput methods for chromatin profiling and 3-D interaction mapping provide rich experimental data sets describing genome organization and dynamics. These data challenge development of new models and algorithms connecting genome architecture with epigenetic marks. In this review, we describe how chromatin architecture could be reconstructed from epigenetic data using biophysical or statistical approaches. We discuss the applicability and limitations of these methods for understanding the mechanisms of chromatin organization. We also highlight the emergence of new predictive approaches for scoring effects of structural variations in human cells.
KW - Hi-C
KW - machine learning
KW - modeling
KW - polymer physics
KW - predicting approaches
UR - http://www.scopus.com/inward/record.url?scp=85100573399&partnerID=8YFLogxK
UR - https://www.mendeley.com/catalogue/368634ae-a940-3f09-a121-abf927840469/
U2 - 10.3389/fgene.2020.617202
DO - 10.3389/fgene.2020.617202
M3 - Review article
C2 - 33552135
AN - SCOPUS:85100573399
VL - 11
JO - Frontiers in Genetics
JF - Frontiers in Genetics
SN - 1664-8021
M1 - 617202
ER -
ID: 27772575