NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Series GSE95816 Query DataSets for GSE95816
Status Public on Mar 09, 2017
Title Whole genome methylation profiling of melanoma-derived induced pluripotent cancer cells in comparison to the parental melanoma cells
Organism Homo sapiens
Experiment type Genome binding/occupancy profiling by genome tiling array
Summary The Illumina Infinium HumanMethylation450 Bead Chip was used to obtain DNA methylation profiles. Samples included melanoma cell lines A375 and HT-144 as well as their reprogrammed progeny and melanoma-iPCC-derived fibroblasts. Pluripotent stem cells and normal human fibroblasts served as references.
 
Overall design Genomic DNA from reprogrammed induced pluripotent cancer cells compared to parental melanoma cells, pluripotent stem cells and iPCC-derived fibroblasts as well as normal human fibroblasts.
 
Contributor(s) Bernhardt M, Utikal J
Citation(s) 28392221
Submission date Mar 08, 2017
Last update date Mar 22, 2019
Contact name Jochen Utikal
Organization name German Cancer Research Center
Department Clinical Cooperation Unit Dermato-Oncology
Lab Utikal Lab
Street address Im Neuenheimer Feld 280
City Heidelberg
ZIP/Postal code 69120
Country Germany
 
Platforms (1)
GPL13534 Illumina HumanMethylation450 BeadChip (HumanMethylation450_15017482)
Samples (29)
GSM2526416 A375_1
GSM2526417 A375_2
GSM2526418 A375_3
Relations
BioProject PRJNA378507

Download family Format
SOFT formatted family file(s) SOFTHelp
MINiML formatted family file(s) MINiMLHelp
Series Matrix File(s) TXTHelp

Supplementary file Size Download File type/resource
GSE95816_GA_illumina_methylation_beta_values.txt.gz 106.6 Mb (ftp)(http) TXT
GSE95816_GA_illumina_methylation_signal_intensities.txt.gz 69.6 Mb (ftp)(http) TXT
GSE95816_RAW.tar 421.3 Mb (http)(custom) TAR (of IDAT)
Processed data included within Sample table
Processed data are available on Series record

| NLM | NIH | GEO Help | Disclaimer | Accessibility |
NCBI Home NCBI Search NCBI SiteMap