NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM2722217 Query DataSets for GSM2722217
Status Public on May 13, 2020
Title Primed state RUES-2 [RUES2-3]
Sample type genomic
 
Source name embryonic stem cells
Organism Homo sapiens
Characteristics cell line: RUES-2
cell type: embryonic stem cells
state: primed state
passages: 30-33
qc: Passed
Growth protocol Human embryonic stem cell (ESC) lines H9,RUES-2 were maintained on mitomycin C-treated mouse embryonic fibroblast (MEF) feeder cells in hESC medium (DMEM/F12 containing 20% knockout serum replacement, 2mM l-glutamine, 1% nonessential amino acids (NEAA), 100U of penicillin, 100 mg of streptomycin (all from Life Technologies), 0.1mM β-mercaptoethanol (Sigma), and 4 ng/mL bFGF (PeproTech). Cells were passaged every 6–7 days by dispase (1 mg/mL, Life Technologies) treatment.
Extracted molecule genomic DNA
Extraction protocol Genomic DNA was extracted and purified using QIAamp DNA Blood Mini Kit according to standard instructions
Label cy3,cy5
Label protocol DNA methylation was determined using Illumina MethylationEPIC array with the Infinium HD Assay Methylation Protocol. 500ng of genomic DNA for each samples is bisulfite converted with Zymo Research EZ DNA Methylation-Gold Kit, then 200ng of each converted sample is amplified and fragmented as per the InfiniumHD Assay Methylation Protocol.
 
Hybridization protocol Samples are resuspended and loaded into the Methylation EPIC BeadChips and hybridized overnight as per the Infinium HD Assay Methylation Protocol.
Scan protocol Following washing, staining, and addition of a protective coating to the BeadChips as per Infinium HD Assay Methylation Protocol, the BeadChips are imaged using the Illumina iScan Reader to measure the fluorescence intensity of each probe for both methylation and unmethylated DNA.
Data processing BeadChip data files are analyzed with Illumina's GenomeStudio (v2011.1) methylation module (v1.9.0) to report control normalization with background subtraction methylation data.
 
Submission date Jul 28, 2017
Last update date May 15, 2020
Contact name Jian Feng
E-mail(s) jianfeng@buffalo.edu
Phone 716-829-2345
Organization name State University of New York at Buffalo
Department Department of Physiology and Biophysics
Lab Feng Lab
Street address 955 Main Street, Room 3102
City Buffalo
State/province NY
ZIP/Postal code 14203
Country USA
 
Platform ID GPL21145
Series (1)
GSE102031 Human Naive Pluripotency Attained by Transient Inhibition of mTOR

Data table header descriptions
ID_REF
VALUE Average Beta
RUES2-3.Signal_A
RUES2-3.Signal_B
RUES2-3.Detection Pval

Data table
ID_REF VALUE RUES2-3.Signal_A RUES2-3.Signal_B RUES2-3.Detection Pval
cg00000029 0.78465 819 3349 0
cg00000103 0.89157 266 3006 0
cg00000109 0.85872 351 2742 0
cg00000155 0.85337 625 4218 0
cg00000158 0.91838 323 4761 0
cg00000165 0.0597 3575 233 0
cg00000221 0.79201 578 2583 0
cg00000236 0.82023 827 4230 0
cg00000289 0.82149 180 1288 0
cg00000292 0.81353 1902 8734 0
cg00000321 0.1322 4400 686 0
cg00000363 0.09424 6839 722 0
cg00000540 0.74287 1812 5523 0
cg00000579 0.89291 493 4942 0
cg00000596 0.72987 2004 5686 0
cg00000622 0.02537 11731 308 0
cg00000658 0.69992 3052 7352 0
cg00000714 0.2682 14635 5400 0
cg00000721 0.85452 465 3317 0
cg00000734 0.08429 10886 1011 0

Total number of rows: 865918

Table truncated, full table size 25830 Kbytes.




Supplementary file Size Download File type/resource
GSM2722217_201172540021_R03C01_Grn.idat.gz 7.0 Mb (ftp)(http) IDAT
GSM2722217_201172540021_R03C01_Red.idat.gz 7.0 Mb (ftp)(http) IDAT
Processed data included within Sample table

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