NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM4272462 Query DataSets for GSM4272462
Status Public on Apr 29, 2021
Title CTRL-C1_Replicate_1
Sample type RNA
 
Source name Lymphoblastoid Cell Line from Control Healthy Individual. Age- and Sex-matched Control for AOA2-P1.
Organism Homo sapiens
Characteristics cell type: Lymphoblastoid Cell Line transformed by Epstein-Barr Virus
morphology: Lymphoblast
genotype: Normal
Treatment protocol Cells were harvested by trypsinization followed by two washes with ice-cold PBS.
Growth protocol Lymphoblastoid cell lines (LCLs) from control and AOA2 patients were cultured in RPMI 1640 medium (ThermoFisher) containing 20% FBS (Sigma-Aldrich), 1% Penicillin/Streptomycin (P/S; Sigma-Aldrich), 2 mM L-glutamine (ThermoFisher) and 1% Non-Essential Amino Acids (ThermoFisher). All LCLs were grown at 37°C and in a humidified atmosphere containing 5% CO2.
Extracted molecule total RNA
Extraction protocol Total RNA was extracted from cultured human and mouse cells using RNeasy Mini Kit (Qiagen) according to the manufacturer’s instruction, including an on-column DNase treatment to eliminate any contaminating genomic DNA.
Label Biotin
Label protocol RNA samples were amplified and biotin labeled using the WT-Ovation Pico target prep v1.0 protocol, which was derived from the NuGEN WT-Ovation Pico RNA Amplification system and the NuGEN FL-Ovation cDNA Biotin Module v2.
 
Hybridization protocol All fragmented and biotin labeled cDNA samples were hybridized to Affymetrix GeneChip Human Gene 1.0 ST microarrays for 16 hr at 45C. Arrays were washed using the Affymetrix Fluidics Station 450 according to the manufacturer’s recommendations.
Scan protocol Scanning was performed using the Affymetrix GeneChip 3000 7G scanner with autoloader running Affymetrix GeneChip Command Console (AGCC) software.
Description Gene expression data from CTRL-C1
Data processing Affymetrix gene expression data was analyzed using Bioconductor 2.5 running on R version 2.10.0. Probeset expression measures were calculated using RMA with the oligo package.
 
Submission date Jan 14, 2020
Last update date Apr 29, 2021
Contact name Steve West
E-mail(s) stephen.west@crick.ac.uk
Organization name The Francis Crick Institute
Street address 1 Midland Road
City London
ZIP/Postal code NW1 1AT
Country United Kingdom
 
Platform ID GPL6244
Series (2)
GSE143574 Integrated Genome and Transcriptome Analyses Reveal the Mechanism of Genome Instability in Ataxia with Oculomotor Apraxia 2
GSE143680 Integrated Genome and Transcriptome Analyses Reveal the Mechanism of Genome Instability in Ataxia with Oculomotor Apraxia 2.

Data table header descriptions
ID_REF
VALUE RMA normalised expression data

Data table
ID_REF VALUE
7892501 2.005124186
7892502 2.767915524
7892503 2.29727796
7892504 7.420058861
7892505 2.457835331
7892506 2.721974547
7892507 3.5128895
7892508 2.417901213
7892509 10.80176555
7892510 2.277306247
7892511 1.773261036
7892512 4.252304893
7892513 2.612669746
7892514 8.940040054
7892515 9.084572402
7892516 3.883457652
7892517 2.461593913
7892518 2.918037913
7892519 4.902406444
7892520 8.4520843

Total number of rows: 33297

Table truncated, full table size 646 Kbytes.




Supplementary file Size Download File type/resource
GSM4272462_CTRL-C1_Rep_1.CEL.gz 3.6 Mb (ftp)(http) CEL
Processed data included within Sample table

| NLM | NIH | GEO Help | Disclaimer | Accessibility |
NCBI Home NCBI Search NCBI SiteMap
External link. Please review our privacy policy.