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Sample GSM5919180 Query DataSets for GSM5919180
Status Public on Jul 25, 2022
Title FSF1_TERT_27
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: 69.67
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 0.123482862003753
cg00000103
cg00000109 0.9262733091842
cg00000155 0.94655094923357
cg00000158 0.956580040680465
cg00000165 0.169572275710273
cg00000221 0.916843235574832
cg00000236 0.932423430351037
cg00000289 0.805684381748545
cg00000292 0.483086922493014
cg00000321 0.736785728397537
cg00000363 0.619133019946821
cg00000540 0.548596312759502
cg00000579 0.960155476622624
cg00000596 0.0609152707168683
cg00000622 0.0238582024918929
cg00000658 0.84774451831792
cg00000714 0.235485736497948
cg00000721 0.831188141293997
cg00000734 0.109201602290546

Total number of rows: 865918

Table truncated, full table size 22561 Kbytes.




Supplementary file Size Download File type/resource
GSM5919180_205138650055_R04C01_Grn.idat.gz 7.0 Mb (ftp)(http) IDAT
GSM5919180_205138650055_R04C01_Red.idat.gz 7.1 Mb (ftp)(http) IDAT
Processed data included within Sample table

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