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Sample GSM2722209 Query DataSets for GSM2722209
Status Public on May 13, 2020
Title Primed state H9 [H9-3]
Sample type genomic
 
Source name embryonic stem cells
Organism Homo sapiens
Characteristics cell line: H9
cell type: embryonic stem cells
state: primed state
passages: 31-35
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
H9-3.Signal_A
H9-3.Signal_B
H9-3.Detection Pval

Data table
ID_REF VALUE H9-3.Signal_A H9-3.Signal_B H9-3.Detection Pval
cg00000029 0.73875 719 2315 0
cg00000103 0.91132 175 2828 0
cg00000109 0.84723 392 2727 0
cg00000155 0.89715 355 3965 0
cg00000158 0.89512 550 5551 0
cg00000165 0.06116 4101 274 0
cg00000221 0.84621 412 2815 0
cg00000236 0.81265 869 4201 0
cg00000289 0.85057 135 1340 0
cg00000292 0.7716 2346 8263 0
cg00000321 0.10604 4570 554 0
cg00000363 0.09608 6877 742 0
cg00000540 0.7326 1982 5705 0
cg00000579 0.89484 467 4827 0
cg00000596 0.81598 1424 6757 0
cg00000622 0.0034 10177 35 0
cg00000658 0.71204 2709 6947 0
cg00000714 0.21098 14583 3926 0
cg00000721 0.84905 511 3434 0
cg00000734 0.08605 10203 970 0

Total number of rows: 865918

Table truncated, full table size 25758 Kbytes.




Supplementary file Size Download File type/resource
GSM2722209_201172540020_R03C01_Grn.idat.gz 7.0 Mb (ftp)(http) IDAT
GSM2722209_201172540020_R03C01_Red.idat.gz 7.1 Mb (ftp)(http) IDAT
Processed data included within Sample table

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