<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>41(8)</volume><submitter>Mullen DJ</submitter><funding>USC Center for Genetic Epidemiology</funding><funding>John H. Richardson Endowed Postdoctoral Fellowship in Oncology Research</funding><funding>USC Keck School of Medicine</funding><funding>USC Norris Comprehensive Cancer Center</funding><pubmed_abstract>&lt;h4>Summary&lt;/h4>There is a lack of publicly available bioinformatic tools that can be widely used by researchers to identify transcription factors (TFs) that regulate cell type-specific regulatory elements (REs). To address this, we developed the Tracing regulatory Element Networks using Epigenetic Traits (TENET) R/Bioconductor package. By collecting hundreds of histone mark and open chromatin datasets from a variety of cell lines, primary cells, and tissues, and comparing these features along with matched DNA methylation and gene expression data, TENET identifies TFs and REs linked to a specific cell type. Moreover, we developed methods to interrogate findings using motifs, clinical information, and other genomic and chromatin conformation capture datasets, and applied them to pan-cancer data, highlighting TFs and REs associated with ten different cancer types. TENET enables researchers to better characterize the 3D epigenomes of cell types of interest for future clinical applications.&lt;h4>Availability and implementation&lt;/h4>TENET is available at http://bioconductor.org/packages/TENET. Curated functional genomic datasets utilized by TENET are available at http://bioconductor.org/packages/TENET.AnnotationHub. Example datasets are available at http://bioconductor.org/packages/TENET.ExperimentHub.</pubmed_abstract><journal>Bioinformatics (Oxford, England)</journal><pagination>btaf435</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12349384</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Tracing regulatory element networks using epigenetic traits to identify key transcription factors: TENET R/Bioconductor package.</pubmed_title><pmcid>PMC12349384</pmcid><pubmed_authors>Wu Z</pubmed_authors><pubmed_authors>Cao H</pubmed_authors><pubmed_authors>Han L</pubmed_authors><pubmed_authors>Nelson-Moore E</pubmed_authors><pubmed_authors>Mullen DJ</pubmed_authors><pubmed_authors>Rhie SK</pubmed_authors><pubmed_authors>Offringa IA</pubmed_authors></additional><is_claimable>false</is_claimable><name>Tracing regulatory element networks using epigenetic traits to identify key transcription factors: TENET R/Bioconductor package.</name><description>&lt;h4>Summary&lt;/h4>There is a lack of publicly available bioinformatic tools that can be widely used by researchers to identify transcription factors (TFs) that regulate cell type-specific regulatory elements (REs). To address this, we developed the Tracing regulatory Element Networks using Epigenetic Traits (TENET) R/Bioconductor package. By collecting hundreds of histone mark and open chromatin datasets from a variety of cell lines, primary cells, and tissues, and comparing these features along with matched DNA methylation and gene expression data, TENET identifies TFs and REs linked to a specific cell type. Moreover, we developed methods to interrogate findings using motifs, clinical information, and other genomic and chromatin conformation capture datasets, and applied them to pan-cancer data, highlighting TFs and REs associated with ten different cancer types. TENET enables researchers to better characterize the 3D epigenomes of cell types of interest for future clinical applications.&lt;h4>Availability and implementation&lt;/h4>TENET is available at http://bioconductor.org/packages/TENET. Curated functional genomic datasets utilized by TENET are available at http://bioconductor.org/packages/TENET.AnnotationHub. Example datasets are available at http://bioconductor.org/packages/TENET.ExperimentHub.</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Aug</publication><modification>2026-04-30T15:46:57.594Z</modification><creation>2026-04-07T16:09:12.842Z</creation></dates><accession>S-EPMC12349384</accession><cross_references><pubmed>40748712</pubmed><doi>10.1093/bioinformatics/btaf435</doi></cross_references></HashMap>