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Sample GSM1910844 Query DataSets for GSM1910844
Status Public on Jan 24, 2017
Title corneal_endothelium_FECD_A39
Sample type RNA
 
Source name corneal endothelium FECD
Organism Homo sapiens
Characteristics rna integrity number: 7.30
gender: female
age: 78 years
tissue: corneal endothelium with Descemet's membrane
group: Fuchs' endothelial corneal dystrophy
type of surgery: Descemet's stripping automated endothelial keratoplasty (DSAEK)
visual acuity: 3/10
pseudophakic?: yes
time between cataract surgery and dsaek: 29 months
Biomaterial provider University Hospitals Leuven (Belgium), Department of Ophthalmology
Treatment protocol The sample was collected in RNAlater.
Growth protocol Not applicable.
Extracted molecule total RNA
Extraction protocol Tissues were disrupted and homogenized manually with a Disposable Pestle (VWRTM International, Radnor, Pennsylvania). RNA extraction was performed with RNeasy® Micro Kit (Qiagen), without DNase treatment.
Label biotin
Label protocol RNA concentration and purity were determined spectrophotometrically using the Nanodrop ND-1000 (Nanodrop Technologies) and RNA integrity was assessed using a Bioanalyser 2100 (Agilent). Using the Ambion WT Expression Kit, per sample, an amount of 100 ng of total RNA spiked with bacterial poly-A RNA positive controls (Affymetrix) was converted to double stranded cDNA in a reverse transcription reaction. Next the sample was converted and amplified to antisense cRNA in an in vitro transcription reaction which was subsequently converted to single stranded sense cDNA. Finally, samples were fragmented and labeled with biotin in a terminal labeling reaction according to the Affymetrix WT Terminal Labeling Kit.
 
Hybridization protocol A mixture of fragmented biotinylated cDNA and hybridisation controls (Affymetrix) was hybridised on Affymetrix GeneChip Human Gene 1.0 ST Arrays followed by staining and washing in a GeneChip® fluidics station 450 (Affymetrix) according to the manufacturer’s procedures.
Scan protocol To assess the raw probe signal intensities, chips were scanned using a GeneChip® scanner 3000 (Affymetrix).
Description corneal endothelium FECD
Data processing Data were processed with RMA (as implemented in the XPS package of Bioconductor). Reported values are on log2-scale.
 
Submission date Oct 19, 2015
Last update date Jan 24, 2017
Contact name Joost J van den Oord
E-mail(s) joost.vandenoord@med.kuleuven.be
Phone +32 16 33 65 91
Organization name KU Leuven
Department Department of Imaging & Pathology
Lab Translational Cell & Tissue Research
Street address Minderbroedersstraat 12, block q, box 1032
City Leuven
ZIP/Postal code 3000
Country Belgium
 
Platform ID GPL6244
Series (2)
GSE74123 Identification of Circulating Fibrocytes and Dendritic Derivatives in Corneal Endothelium of Patients with Fuchs' Dystrophy [microarray expression analysis]
GSE75676 Identification of Circulating Fibrocytes and Dendritic Derivatives in Corneal Endothelium of Patients with Fuchs' Dystrophy

Data table header descriptions
ID_REF
VALUE log2 RMA

Data table
ID_REF VALUE
7892796 13.2363042568903
7892925 10.2727580706667
7893130 11.652401343282
7893306 8.28046921071362
7893613 9.50619648583321
7893939 9.16103107980924
7894584 5.58475810444529
7894611 7.79768097779059
7894970 13.593017561153
7895139 6.91296116987931
7895220 10.7439423868813
7896160 10.0036725033917
7896366 12.6709637847591
7896687 7.46376139717732
7896688 6.3085538255239
7896689 6.2715302587281
7896690 6.36756851403036
7896691 6.14832811041469
7896692 7.55331441992127
7896693 4.23232306524079

Total number of rows: 28886

Table truncated, full table size 702 Kbytes.




Supplementary file Size Download File type/resource
GSM1910844_hyb8265.CEL.gz 4.1 Mb (ftp)(http) CEL
Processed data included within Sample table

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