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Sample GSM5919005 Query DataSets for GSM5919005
Status Public on Jul 25, 2022
Title NFF2_17
Sample type genomic
 
Source name Foreskin
Organism Homo sapiens
Characteristics subexperiment: Baseline profiling
coriell_id: AG21859
cell_line: Neonatal_foreskin_fibroblast_2
donor_age: 0 years
donor_sex: male
culture_oxygen: Ambient
culture_agent: NA
culture_pctfbs: Full
expression_vector: NA
subculture: a
population_doublings: 30.10688632
days_in_culture: 27
batch_date: 05.25.18
growth protocol: Fibroblasts were maintained in Ham’s F12/DMEM 1:1 media supplemented with 10% v/v fetal bovine serum. Triplicate cultures derived from the same parent plate or vial obtained from Coriell were maintained in parallel through replicative senescence, which was defined in this study as drastically slowed growth (inability to reach near-confluence at 14 days after previous passage) or viable fraction of cells falling below 60%. Passaging occurred as cells became approximately 90% confluent.
Extracted molecule genomic DNA
Extraction protocol Frozen cell pellets were thawed and lysed using QIAshredder spin columns (Qiagen). Genomic DNA was extracted from each sample using the AllPrep DNA/RNA Mini Kit (Qiagen), then stored at -80°C before analysis.
Label Cy3 and Cy5
Label protocol Cy3 and Cy5
 
Hybridization protocol Bisulfite-converted DNA was amplified, fragmented, and hybridized to Illumina Infinium Human Methylation850k Beadchip using standard Illumina protocol.
Scan protocol Arrays were imaged using BeadArray Reader (Illumina HiSeq2000) using standard recommended Illumina scanner setting
Data processing Raw IDATs were processed with R (v4.1.1) package ‘SeSAMe’ with noob background correction, non-linear dye bias correction, and non-detection masking. P-value threshold was set at 0.1. Probe masking was performed using the standard mask list in SeSAMe, including probes that overlap with SNPs and repeat elements.
 
Submission date Feb 26, 2022
Last update date Jul 28, 2022
Contact name Peter W Laird
E-mail(s) Peter.Laird@vai.org
Organization name Van Andel Institute
Department Epigenetics
Lab Peter W Laird
Street address 333 Bostwick Ave NE
City Grand Rapids
State/province MI
ZIP/Postal code 49503
Country USA
 
Platform ID GPL23976
Series (2)
GSE197512 Cell division drives DNA methylation loss in late-replicating domains in primary human cells [methylation array]
GSE197545 Cell division drives DNA methylation loss in late-replicating domains in primary human cells

Data table header descriptions
ID_REF
VALUE beta

Data table
ID_REF VALUE
cg00000029 0.588567818338396
cg00000103
cg00000109 0.925613794522968
cg00000155 0.957585917022958
cg00000158 0.967587671119399
cg00000165 0.142503610221325
cg00000221 0.904731514738461
cg00000236 0.818744993530305
cg00000289 0.88576846784683
cg00000292 0.544730493015815
cg00000321 0.212557251467325
cg00000363 0.183440489053054
cg00000540 0.734843557753866
cg00000579 0.930624291639355
cg00000596 0.256342559679416
cg00000622 0.0192472116782341
cg00000658 0.825126816574304
cg00000714 0.166528612507808
cg00000721 0.877574621644614
cg00000734 0.112570818971738

Total number of rows: 865918

Table truncated, full table size 17774 Kbytes.




Supplementary file Size Download File type/resource
GSM5919005_202225190185_R01C01_Grn.idat.gz 6.9 Mb (ftp)(http) IDAT
GSM5919005_202225190185_R01C01_Red.idat.gz 7.1 Mb (ftp)(http) IDAT
Processed data included within Sample table

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