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Sample GSM5919179 Query DataSets for GSM5919179
Status Public on Jul 25, 2022
Title FSF1_TERT_26
Sample type genomic
 
Source name Skin, sacrum
Organism Homo sapiens
Characteristics subexperiment: TERT immortalization
coriell_id: AG06561
cell_line: Fetal_skin_fibroblast_1
donor_age: 16 fetal weeks
donor_sex: female
culture_oxygen: Ambient
culture_agent: NA
culture_pctfbs: Full
expression_vector: TERT
subculture: 2b
population_doublings: 69.32
days_in_culture: 124
batch_date: 05.27.21
growth protocol: Fibroblasts were maintained in Eagle’s MEM with Earle’s salts and non-essential amino acids with 15% 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.
treatment protocol: Low-PD primary fibroblasts were transduced with purified lentiviral particles containing expression vectors encoding human Telomerase Reverse Transcriptase (TERT) and hygromycin resistance marker. Following selection with 250ug/ml hygromycin B, cells were serially cultured in perpetuity, in triplicate.
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 0.586204310695346
cg00000103
cg00000109 0.888850971191996
cg00000155 0.951871217835117
cg00000158 0.961605200950312
cg00000165 0.155538244127887
cg00000221 0.907364796249586
cg00000236 0.922986268807036
cg00000289 0.872711473011527
cg00000292 0.800758710289582
cg00000321 0.452891470688446
cg00000363 0.656248824078777
cg00000540 0.486179742917519
cg00000579 0.964331129950719
cg00000596 0.098059389746316
cg00000622 0.0222134629875528
cg00000658 0.852560179477074
cg00000714 0.218195431285392
cg00000721 0.891702801434136
cg00000734 0.100662009247833

Total number of rows: 865918

Table truncated, full table size 22669 Kbytes.




Supplementary file Size Download File type/resource
GSM5919179_205138650055_R05C01_Grn.idat.gz 7.0 Mb (ftp)(http) IDAT
GSM5919179_205138650055_R05C01_Red.idat.gz 7.1 Mb (ftp)(http) IDAT
Processed data included within Sample table

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