Identification of differentially methylated regions in rare diseases from a single-patient perspective

DNA methylation (5-mC) is being widely recognized as an alternative in the detection of sequence variants in the diagnosis of some rare neurodevelopmental and imprinting disorders. Identification of alteration...

Source: Clinical Epigenetics - December 16, 2022 Category: Research Authors: Robin Grolaux, Alexis Hardy, Catharina Olsen, Sonia Van Dooren, Guillaume Smits and Matthieu Defrance Tags: Research Source Type: research