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Sample GSM955093 Query DataSets for GSM955093
Status Public on Jul 04, 2012
Title donor heart tissue [VC-H3]
Sample type RNA
 
Source name human heart tissue from left ventricular free wall of organ donors with no previous history of heart disease
Organism Homo sapiens
Characteristics rs1333049 genotype: GC
age: 43
Sex: M
batch: 8
Treatment protocol Heart specimens were rapidly frozen in liquid nitrogen at the time of harvest and stored at -80°C until use.
Extracted molecule total RNA
Extraction protocol Total RNA and genomic DNA was simultaneously extracted from frozen tissue after automated grinding (Retsch Mixer Mill MM301, Haan, Germany) in TRIzol® (Invitrogen, Carlsbad, CA) and chloroform. RNA was purified using RNeasy Midi columns (Qiagen, Valencia, CA) according to manufacturer’s instructions and tested for quality and quantity with an Experion (Bio-Rad Laboratories, Hercules, CA). Genomic DNA was extracted from the remaining organic and interphase layers of the TRIzol® extract (see protocol at http://genome-www.stanford.edu/DFSP/materials.shtml).
Label biotin
Label protocol Biotinylated cDNA was prepared according to the standard Affymetrix protocol from 100 ng of total RNA ( whole transcript(WT) sense target labeling assay Technical manual version 4 2007, Affymetrix)) using the non ribosomal RNA reduced option. (chapter 4)
 
Hybridization protocol Following fragmentation, 5.5 ug of single stranded cDNA was hybridized for 17 hr at 45C on GeneChip Human Gene 1.0 ST Array. GeneChips were washed and stained in the Affymetrix Fluidics Station 450.
Scan protocol GeneChips were scanned using the Affymetrix GeneChip Scanner G7 plus.
Description Gene expression and genotype in normal heart
Data processing The data were analysed using R version 2.8.1 with Bioconductor. Aroma Affymetrix was used for background correction, quantile normalization and fitting GCRMA probe level models. Batch effects were corrected with Combat. Limma was used to calculate differential expression and apply Benjamini and Hochberg corection for multiple testing.
 
Submission date Jul 03, 2012
Last update date Jul 04, 2012
Contact name Anna P Pilbrow
E-mail(s) [email protected]
Organization name University of Otago Christchurch
Department Medicine
Lab Christchurch Cardioendocrine Research Group
Street address 2 Riccarton Avenue
City Christchurch
ZIP/Postal code 8041
Country New Zealand
 
Platform ID GPL6244
Series (1)
GSE22253 Gene expression and genotype in normal heart

Data table header descriptions
ID_REF
VALUE GCRMA

Data table
ID_REF VALUE
7892501 4.784756185
7892502 4.377982336
7892503 4.059017891
7892504 8.830987887
7892505 2.540066448
7892506 4.605723272
7892507 4.100701726
7892508 4.879825345
7892509 10.91089251
7892510 2.801613596
7892511 3.332962507
7892512 6.836859675
7892513 4.144939161
7892514 9.446010042
7892515 9.837497458
7892516 3.653924101
7892517 5.662813835
7892518 2.133195608
7892519 4.442020855
7892520 8.685081366

Total number of rows: 33252

Table truncated, full table size 645 Kbytes.




Supplementary file Size Download File type/resource
GSM955093_VC-H3.CEL.gz 6.5 Mb (ftp)(http) CEL
Processed data included within Sample table

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