<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Lu W</submitter><funding>Fundamental Research Funds for the Central Universities</funding><funding>National Key R&amp;amp;D Program of China</funding><funding>National Key R&amp;D Program of China</funding><funding>Opening Research Fund from Shanghai Key Laboratory of Stomatology, Shanghai Ninth People’s Hospital, College of Stomatology, Shanghai Jiao Tong University School of Medicine</funding><funding>Zhejiang Provincial Natural Science Foundation of China</funding><funding>National Natural Science Foundation of China</funding><funding>Opening Research Fund from Shanghai Key Laboratory of Stomatology, Shanghai Ninth People's Hospital, College of Stomatology, Shanghai Jiao Tong University School of Medicine</funding><pagination>bbae373</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11285185</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>25(5)</volume><pubmed_abstract>Histone modifications, known as histone marks, are pivotal in regulating gene expression within cells. The vast array of potential combinations of histone marks presents a considerable challenge in decoding the regulatory mechanisms solely through biological experimental approaches. To overcome this challenge, we have developed a method called CatLearning. It utilizes a modified convolutional neural network architecture with a specialized adaptation Residual Network to quantitatively interpret histone marks and predict gene expression. This architecture integrates long-range histone information up to 500Kb and learns chromatin interaction features without 3D information. By using only one histone mark, CatLearning achieves a high level of accuracy. Furthermore, CatLearning predicts gene ex</pubmed_abstract><journal>Briefings in bioinformatics</journal><pubmed_title>CatLearning: highly accurate gene expression prediction from histone mark.</pubmed_title><pmcid>PMC11285185</pmcid><funding_grant_id>2022YFA1302800</funding_grant_id><funding_grant_id>LZ24C060001</funding_grant_id><funding_grant_id>2019QN81005</funding_grant_id><funding_grant_id>32361133547, 32370613, 32222017, and 81874153</funding_grant_id><funding_grant_id>2022SKLS-KFKT002</funding_grant_id><pubmed_authors>Liu Y</pubmed_authors><pubmed_authors>Shuai Q</pubmed_authors><pubmed_authors>Lu W</pubmed_authors><pubmed_authors>Lin S</pubmed_authors><pubmed_authors>Fang D</pubmed_authors><pubmed_authors>Zhang R</pubmed_authors><pubmed_authors>Tang Y</pubmed_authors><pubmed_authors>Cheng Y</pubmed_authors><pubmed_authors>Liang B</pubmed_authors></additional><is_claimable>false</is_claimable><name>CatLearning: highly accurate gene expression prediction from histone mark.</name><description>Histone modifications, known as histone marks, are pivotal in regulating gene expression within cells. The vast array of potential combinations of histone marks presents a considerable challenge in decoding the regulatory mechanisms solely through biological experimental approaches. To overcome this challenge, we have developed a method called CatLearning. It utilizes a modified convolutional neural network architecture with a specialized adaptation Residual Network to quantitatively interpret histone marks and predict gene expression. This architecture integrates long-range histone information up to 500Kb and learns chromatin interaction features without 3D information. By using only one histone mark, CatLearning achieves a high level of accuracy. Furthermore, CatLearning predicts gene ex</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Jul</publication><modification>2026-06-01T06:55:38.002Z</modification><creation>2026-04-08T10:20:10.713Z</creation></dates><accession>S-EPMC11285185</accession><cross_references><pubmed>39073831</pubmed><doi>10.1093/bib/bbae373</doi></cross_references></HashMap>