A survey of rare epigenetic variation in 23,116 human genomes identifies disease-relevant epivariations and novel CGG expansions
Publication
Date: 26th March 2020 | Source: BioRxiv
Authors: Paras Garg, Bharati Jadhav, Oscar L. Rodriguez, Nihir Patel, Alejandro Martin-Trujillo, Miten Jain, Sofie Metsu, Hugh Olsen, Benedict Paten, Beate Ritz, R. Frank Kooy, Jozef Gecz, Andrew J. Sharp.