| Literature DB >> 29224145 |
Karolina A Aberg1, Robin F Chan1, Linying Xie1, Andrey A Shabalin1, Edwin J C G van den Oord2.
Abstract
Detailed biological knowledge about the potential importance of the methylome is typically lacking for common diseases. Therefore, methylome-wide association studies (MWAS) are critical to detect disease relevant methylation sites. Methyl-CpG-binding domain sequencing (MBD-seq) offers potential advantages compared to antibody-based enrichment, but performance depends critically on using an optimal protocol. Using an optimized protocol, MBD-seq can approximate the sensitivity/specificity obtained with whole-genome bisulfite sequencing, but at a fraction of the costs and time to complete the project. Thus, MBD-seq offers a comprehensive first pass at the CpG methylome and is economically feasible with the samples sizes required for MWAS.Entities:
Keywords: Affinity-based capture; Blood spots; CpG; Differentially methylated regions; High-dimensional data analysis; MBD-seq; MWAS; Methyl-CpG-binding domain; MethylMiner; Methylome-wide association studies; RaMWAS; Sequencing
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Year: 2018 PMID: 29224145 DOI: 10.1007/978-1-4939-7481-8_10
Source DB: PubMed Journal: Methods Mol Biol ISSN: 1064-3745