Title :
Targeted profiling of 5-(hydroxy)methylcytosine in genomic DNA from human livers: Next-generation sequencing of target enriched DNA reveals unexpectedly high interindividual variability of cytosine methylation and hydroxymethylation
Author :
Ivanov, Maxim ; Ingelman-Sundberg, Magnus ; Kals, Mart ; Milani, Lili
Author_Institution :
Dept. of Physiol. & Pharmacology, Karolinska Institutet, Stockholm, Sweden
Abstract :
So far, bisulfite sequencing has been considered as the “gold standard” method for the detection of DNA methylation. The results of whole-genome bisulfite next-generation sequencing (WG-BS-Seq) allowed scientists to conclude that the vast majority of CpG sites in genomic DNA from human and animal tissues are invariably hypermethylated. Only a small proportion (≤ 10-15%) of CpG sites was found to manifest variable degree of methylation between different tissues or among individuals. Moreover, such variably methylated CpG sites were believed to occur almost exclusively within extended clusters (differentially methylated regions, or DMRs).
Keywords :
DNA; biochemistry; bioinformatics; biological tissues; data analysis; genomics; hydrogen compounds; liver; medical computing; molecular biophysics; molecular configurations; molecule-molecule reactions; negative ions; reaction kinetics; sequences; 5-(hydroxy)methylcytosine; CpG site methylation degree; DMR; DNA methylation detection; HSO3-; WG-BS-Seq; animal tissue; bisulfite sequencing; cytosine methylation; differentially methylated region; genomic DNA; human liver; human tissue; hydroxymethylation; hypermethylation; interindividual variability; target enriched DNA; targeted profiling; variable CpG site methylation; whole-genome bisulfite next-generation sequencing; Bioinformatics; DNA; Genomics; Liver; Next generation networking; Protocols; Sequential analysis;
Conference_Titel :
Bioinformatics and Biomedicine (BIBM), 2014 IEEE International Conference on
Conference_Location :
Belfast
DOI :
10.1109/BIBM.2014.6999389