NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM955063 Query DataSets for GSM955063
Status Public on Jul 04, 2012
Title donor heart tissue [VC-F5]
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: GG
age: 66
Sex: F
batch: 9
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) anna.pilbrow@otago.ac.nz
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 2.283677495
7892502 4.150696956
7892503 4.156022234
7892504 8.218899478
7892505 2.83126419
7892506 2.87909317
7892507 4.102163609
7892508 3.704401101
7892509 11.03441965
7892510 3.725058289
7892511 3.333900726
7892512 6.766971491
7892513 2.838390578
7892514 8.610150563
7892515 9.832371515
7892516 2.59577758
7892517 5.635472308
7892518 2.190146174
7892519 4.897238529
7892520 8.468874054

Total number of rows: 33252

Table truncated, full table size 645 Kbytes.




Supplementary file Size Download File type/resource
GSM955063_VC-F5.CEL.gz 3.9 Mb (ftp)(http) CEL
Processed data included within Sample table

| NLM | NIH | GEO Help | Disclaimer | Accessibility |
NCBI Home NCBI Search NCBI SiteMap