Comment[ArrayExpressAccession] E-GEOD-44918 MAGE-TAB Version 1.1 Public Release Date 2014-12-08 Investigation Title High resolution nulceotide level methylation map of female mouse primary keratinocytes Comment[Submitted Name] High resolution nulceotide level methylation map of female mouse primary keratinocytes Experiment Description We determined the high resolution methylation maps of female mouse primary keratinocytes and compared these maps at nucleotide level with the female mouse primary dermal fibroblasts. Single nucleotide level methylation maps led us to identify several additional features of CG methylation. We have detected that differentially methylated regions are epigenetically marked in other cells including embryonic stem cells and neuronal progeniator cells. Different new charecteristics and functions were also discovered with these methylation maps. Determinationof whole genome DNA methylation profiles (BS-seq) of primary mouse keratinocytes Term Source Name ArrayExpress EFO Term Source File http://www.ebi.ac.uk/arrayexpress/ http://www.ebi.ac.uk/efo/efo.owl Person Last Name Chatterjee Chatterjee Vinson Person First Name Raghunath Raghunath Charles Person Email raghuchatterjee@gmail.com Person Affiliation NCI, NIH Person Address LM, NCI, NIH, 9000 Rockville Pike, Bldg. 37/ 3128, Bethesda, MD, USA Person Roles submitter Protocol Name P-GSE44918-3 P-GSE44918-2 P-GSE44918-1 Protocol Description Illumina RTA 1.7.45 and Casava 1.8 were used for base calling Novoalign Bisulfite module was used for mapping to the mouse assembly mm9 The base calls per reference position on each strand were used to identify methylated cytosines in the context of CpG, CHG and CHH. Genome_build: mm9 Supplementary_files_format_and_content: tab-delimited text files include methylation percent for mouse keratinocytes Primary mouse keratinicytes were cultured for 3 days. DNA was extractes using Qiagen DNA purification kit from the primary cells. . Methylome libraries were prepared for sequencing using standard Illumina protocols Primary mouse keratinocytes were cultured for 3 days in SMEM medium (Invitrogen) with 10% chealetd FBS. Protocol Type normalization data transformation protocol nucleic acid library construction protocol growth protocol Comment[SecondaryAccession] GSE44918 Comment[GEOReleaseDate] 2014-12-08 Comment[ArrayExpressSubmissionDate] 2013-03-06 Comment[GEOLastUpdateDate] 2014-12-08 Comment[AEExperimentType] methylation profiling by high throughput sequencing Comment[SecondaryAccession] SRP018963 Comment[SequenceDataURI] http://www.ebi.ac.uk/ena/data/view/SRR768516-SRR768523 SDRF File E-GEOD-44918.sdrf.txt