Literature DB >> 32623772

EpigenCentral: Portal for DNA methylation data analysis and classification in rare diseases.

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/.
© 2020 Wiley Periodicals LLC.

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


  4 in total

Review 1.  Anatomy of DNA methylation signatures: Emerging insights and applications.

Authors:  Eric Chater-Diehl; Sarah J Goodman; Cheryl Cytrynbaum; Andrei L Turinsky; Sanaa Choufani; Rosanna Weksberg
Journal:  Am J Hum Genet       Date:  2021-07-22       Impact factor: 11.025

Review 2.  Epigenomic Approaches for the Diagnosis of Rare Diseases.

Authors:  Beatriz Martinez-Delgado; Maria J Barrero
Journal:  Epigenomes       Date:  2022-07-27

Review 3.  Strategies to Uplift Novel Mendelian Gene Discovery for Improved Clinical Outcomes.

Authors:  Eleanor G Seaby; Heidi L Rehm; Anne O'Donnell-Luria
Journal:  Front Genet       Date:  2021-06-17       Impact factor: 4.599

4.  The utility of DNA methylation signatures in directing genome sequencing workflow: Kabuki syndrome and CDK13-related disorder.

Authors:  Ashish Marwaha; Gregory Costain; Cheryl Cytrynbaum; Roberto Mendoza-Londono; Lauren Chad; Zain Awamleh; Eric Chater-Diehl; Sanaa Choufani; Rosanna Weksberg
Journal:  Am J Med Genet A       Date:  2022-01-18       Impact factor: 2.578

  4 in total

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