| Literature DB >> 35616708 |
Ali Javadmanesh1,2, Afsaneh Mojtabanezhad Shariatpanahi2, Ehsan Shams Davodly2, Marjan Azghandi1,2, Maryam Yassi2, Mehdi Heidari2, Matin Kerachian3,4, Mohammad Amin Kerachian5,6,7.
Abstract
DNA methylation is a fundamental epigenetic process and have a critical role in many biological processes. The study of DNA methylation at a large scale of genomic levels is widely conducted by several techniques that are next-generation sequencing (NGS)-based methods. Methylome data revealed by DNA methylation next-generation sequencing (mNGS), should be always verified by another technique which they usually have a high cost. In this study, we offered a low-cost approach to corroborate the mNGS data. In this regard, mNGS was performed on 6 colorectal cancer (case group) and 6 healthy individual colon tissue (control group) samples. An R-script detected differentially methylated regions (DMRs), was further validated by high resolution melting (MS-HRM) analysis. After analyzing the data, the algorithm found 194 DMRs. Two locations with the highest level of methylation difference were verified by MS-HRM, which their results were in accordance with the mNGS. Therefore, in the present study, we suggested MS-HRM as a simple, accurate and low-cost method, useful for confirming methylation sequencing results.Entities:
Keywords: Bisulfite; DNA Methylation Sequencing; High resolution melting; Validation
Mesh:
Year: 2022 PMID: 35616708 DOI: 10.1007/s00438-022-01906-1
Source DB: PubMed Journal: Mol Genet Genomics ISSN: 1617-4623 Impact factor: 3.291