| Literature DB >> 32623772 |
Andrei L Turinsky1,2, Sanaa Choufani1, Kevin Lu1,2, Da Liu1,2, Pouria Mashouri1,2, Daniel Min1,2, Rosanna Weksberg1,3,4,5,6, Michael Brudno1,2,7,8.
Abstract
Epigenetic processes play a key role in regulating gene expression. Genetic variants that disrupt chromatin-modifying proteins are associated with a broad range of diseases, some of which have specific epigenetic patterns, such as aberrant DNA methylation (DNAm), which may be used as disease biomarkers. While much of the epigenetic research has focused on cancer, there is a paucity of resources devoted to neurodevelopmental disorders (NDDs), which include autism spectrum disorder and many rare, clinically overlapping syndromes. To address this challenge, we created EpigenCentral, a free web resource for biomedical researchers, molecular diagnostic laboratories, and clinical practitioners to perform the interactive classification and analysis of DNAm data related to NDDs. It allows users to search for known disease-associated patterns in their DNAm data, classify genetic variants as pathogenic or benign to assist in molecular diagnostics, or analyze patterns of differential methylation in their data through a simple web form. EpigenCentral is freely available at http://epigen.ccm.sickkids.ca/.Entities:
Keywords: DNA methylation; epigenetics; neurodevelopmental disorders; pathogenicity prediction; rare diseases; variant classification
Mesh:
Year: 2020 PMID: 32623772 DOI: 10.1002/humu.24076
Source DB: PubMed Journal: Hum Mutat ISSN: 1059-7794 Impact factor: 4.878