{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"omics_type":["Unknown"],"volume":["10(7)"],"submitter":["Hing B"],"pubmed_abstract":["Methyl-Seq was recently developed as a targeted approach to assess DNA methylation (DNAm) at a genome-wide level in human. We adapted it for mouse and sought to examine DNAm differences across liver and 2 brain regions: cortex and hippocampus. A custom hybridization array was designed to isolate 99 Mb of CpG islands, shores, shelves, and regulatory elements in the mouse genome. This was followed by bisulfite conversion and sequencing on the Illumina HiSeq2000. The majority of differentially methylated cytosines (DMCs) were present at greater than expected frequency in introns, intergenic regions, near CpG islands, and transcriptional enhancers. Liver-specific enhancers were observed to be methylated in cortex, while cortex specific enhancers were methylated in the liver. Interestingly, com"],"journal":["Epigenetics"],"pagination":["581-96"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC4622595"],"repository":["biostudies-literature"],"pubmed_title":["Adaptation of the targeted capture Methyl-Seq platform for the mouse genome identifies novel tissue-specific DNA methylation patterns of genes involved in neurodevelopment."],"pmcid":["PMC4622595"],"pubmed_authors":["Hing B","Potash JB","Jancic D","Druley TE","McKane M","Braun P","Tamashiro KL","Lee RS","Michaelson JJ","Ramos E"],"additional_accession":[]},"is_claimable":false,"name":"Adaptation of the targeted capture Methyl-Seq platform for the mouse genome identifies novel tissue-specific DNA methylation patterns of genes involved in neurodevelopment.","description":"Methyl-Seq was recently developed as a targeted approach to assess DNA methylation (DNAm) at a genome-wide level in human. We adapted it for mouse and sought to examine DNAm differences across liver and 2 brain regions: cortex and hippocampus. A custom hybridization array was designed to isolate 99 Mb of CpG islands, shores, shelves, and regulatory elements in the mouse genome. This was followed by bisulfite conversion and sequencing on the Illumina HiSeq2000. The majority of differentially methylated cytosines (DMCs) were present at greater than expected frequency in introns, intergenic regions, near CpG islands, and transcriptional enhancers. Liver-specific enhancers were observed to be methylated in cortex, while cortex specific enhancers were methylated in the liver. Interestingly, com","dates":{"release":"2015-01-01T00:00:00Z","publication":"2015","modification":"2025-04-29T10:57:06.963Z","creation":"2019-03-27T02:00:52Z"},"accession":"S-EPMC4622595","cross_references":{"pubmed":["25985232"],"doi":["10.1080/15592294.2015.1045179"]}}