NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM1379937 Query DataSets for GSM1379937
Status Public on Jan 01, 2015
Title C02109 Idiopathic Dilated CMP Left Ventricle
Sample type RNA
 
Source name heart left ventricle, idiopathic dilated CMP
Organism Homo sapiens
Characteristics tissue: heart left ventricle
heart failure: yes
disease status: idiopathic dilated CMP
gender: male
age: 58
Treatment protocol Explanted myocardium snap frozen in liquid nitrogen.
Growth protocol None
Extracted molecule total RNA
Extraction protocol Trizol extraction of total RNA was performed according to the manufacturer's instructions.
Label biotin
Label protocol 100ng of total RNA was converted to first-strand cDNA using reverse transcriptase primed by a poly(T) oligomer that incorporated the T7 RNA polymerase promoter. Second-strand cDNA synthesis was followed by in vitro transcription (Affymetrix One-Cycle Target Labeling Kit) for linear amplification and biotinylation of each transcript.
 
Hybridization protocol cDNAs were added to Affymetrix hybridization cocktails, heated at 99ºC for 2 min and hybridized for 16 h at 45ºC to Affymetrix Human Gene 1.1 ST Array GeneChips (Affymetrix Inc., Santa Clara, CA). The microarrays were then washed at low (6X SSPE) and high (100mM MES, 0.1M NaCl) stringency and stained with streptavidin-phycoerythrin. Fluorescence was amplified by adding biotinylated anti-streptavidin and an additional aliquot of streptavidin-phycoerythrin stain.
Scan protocol A confocal scanner was used to collect fluorescence signal after excitation at 570 nm.
Description C02109
PolyA mRNA
Data processing Microarray data were analyzed using the Oligo package available at the Bioconductor website (www.bioconductor.org). The raw data were first background-corrected by the Robust Multichip Average (RMA) method and then normalized by an invariant set method. Microarray Processing batch were controlled for using the R package Combat. Differential gene expression was analyzed by the Limma package available at the Bioconductor website. P-values obtained from the multiple comparison tests were corrected by false discovery rates.
 
Submission date May 06, 2014
Last update date Jan 01, 2015
Contact name Michael Patrick Morley
E-mail(s) mmorley@pennmedicine.upenn.edu
Phone 215-898-2026
Organization name Perelman School of Medicine at the University of Pennsylvania
Department Penn Cardiovascular Institute
Street address 3400 Civic Center Blvd, Bldg 421
City Philadelphia
State/province PA
ZIP/Postal code 19104
Country USA
 
Platform ID GPL11532
Series (2)
GSE57338 RNA-Seq Identifies Novel Myocardial Gene Expression Signatures of Heart Failure [microarray]
GSE57345 RNA-Seq Identifies Novel Myocardial Gene Expression Signatures of Heart Failure

Data table header descriptions
ID_REF
VALUE RMA log2 signal

Data table
ID_REF VALUE
7892501 2.35375964
7892502 3.567448956
7892503 2.912221345
7892504 7.112006011
7892505 3.492678247
7892506 3.373155373
7892507 4.333241116
7892508 5.98110945
7892509 9.651644825
7892510 4.244955143
7892511 3.476242666
7892512 5.164023842
7892513 2.773079558
7892514 9.157439423
7892515 8.319680445
7892516 2.420022758
7892517 5.081040164
7892518 3.725042027
7892519 3.737074879
7892520 7.829272857

Total number of rows: 33297

Table truncated, full table size 646 Kbytes.




Supplementary file Size Download File type/resource
GSM1379937_C02109_HuGene1.1ST.CEL.gz 4.5 Mb (ftp)(http) CEL
Processed data included within Sample table

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