Whole human genome 5'-mC methylation analysis using long read nanopore sequencing.
Ontology highlight
ABSTRACT: Methylation microarray and bisulphite sequencing are often used to study 5'-methylcytosine (5'-mC) modification of CpG dinucleotides in the human genome. Although both technologies produce trustworthy results, the evaluation of the methylation status of CpG sites suffers from the potential side effects of DNA modification by bisulphite and/or the ambiguity of mapping short reads in repetitive and highly homologous genomic regions, respectively. Nanopore sequencing is an attractive alternative for the study of 5'-mC since it allows sequencing of native DNA molecules, whereas the long reads produced by this technology help to increase the resolution of those genomic regions. In this work, we show that nanopore sequencing with 10X coverage depth, using DNA from a human cell line, produces 5'-
SUBMITTER: Silva C
PROVIDER: S-EPMC9665147 | biostudies-literature | 2022 Dec
REPOSITORIES: biostudies-literature
ACCESS DATA