NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM5919202 Query DataSets for GSM5919202
Status Public on Jul 25, 2022
Title FSF1_TERT_49
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: 2a
population_doublings: 121.85
days_in_culture: 221
batch_date: 09.24.21
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
cg00000103
cg00000109 0.912929058276181
cg00000155 0.960609889224532
cg00000158 0.956871740222661
cg00000165 0.319505823549997
cg00000221 0.888688674355916
cg00000236 0.925135751575182
cg00000289
cg00000292 0.615240834673277
cg00000321 0.743266419262961
cg00000363 0.705959995243848
cg00000540 0.457244439836552
cg00000579 0.943651289207687
cg00000596 0.0660503637357724
cg00000622 0.0217963129506677
cg00000658 0.870065432320519
cg00000714 0.375955181370777
cg00000721 0.802726813199768
cg00000734 0.0646524574551875

Total number of rows: 865918

Table truncated, full table size 22008 Kbytes.




Supplementary file Size Download File type/resource
GSM5919202_205589740160_R02C01_Grn.idat.gz 6.9 Mb (ftp)(http) IDAT
GSM5919202_205589740160_R02C01_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