<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Lamberti WF</submitter><funding>National Institutes of Health</funding><funding>National Institute of General Medical Sciences</funding><pagination>3387-3398</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9260447</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>20</volume><pubmed_abstract>Higher-order chromatin structures have functional impacts on gene regulation and cell identity determination. Using high-throughput sequencing (HTS)-based methods like Hi-C, active or inactive compartments and open or closed topologically associating domain (TAD) structures can be identified on a cell population level. Recently developed high-resolution three-dimensional (3D) molecular imaging techniques such as 3D electron microscopy with in situ hybridization (3D-EMSIH) and 3D structured illumination microscopy (3D-SIM) enable direct detection of physical representations of chromatin structures in a single cell. However, computational analysis of 3D image data with explainability and interpretability on functional characteristics of chromatin structures is still challenging. We developed</pubmed_abstract><journal>Computational and structural biotechnology journal</journal><pubmed_title>Extracting physical characteristics of higher-order chromatin structures from 3D image data.</pubmed_title><pmcid>PMC9260447</pmcid><funding_grant_id>R35GM133712</funding_grant_id><pubmed_authors>Lamberti WF</pubmed_authors><pubmed_authors>Zang C</pubmed_authors></additional><is_claimable>false</is_claimable><name>Extracting physical characteristics of higher-order chromatin structures from 3D image data.</name><description>Higher-order chromatin structures have functional impacts on gene regulation and cell identity determination. Using high-throughput sequencing (HTS)-based methods like Hi-C, active or inactive compartments and open or closed topologically associating domain (TAD) structures can be identified on a cell population level. Recently developed high-resolution three-dimensional (3D) molecular imaging techniques such as 3D electron microscopy with in situ hybridization (3D-EMSIH) and 3D structured illumination microscopy (3D-SIM) enable direct detection of physical representations of chromatin structures in a single cell. However, computational analysis of 3D image data with explainability and interpretability on functional characteristics of chromatin structures is still challenging. We developed</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022</publication><modification>2025-04-04T03:06:08.073Z</modification><creation>2025-04-04T03:06:08.073Z</creation></dates><accession>S-EPMC9260447</accession><cross_references><pubmed>35832633</pubmed><doi>10.1016/j.csbj.2022.06.018</doi></cross_references></HashMap>