NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM1060905 Query DataSets for GSM1060905
Status Public on Mar 04, 2013
Title G1E_D218Y, biological rep 3
Sample type RNA
 
Source name GATA1-null G1E_GATA1(D218Y)-ER
Organism Mus musculus
Characteristics cell line background: G1E
cell type: GATA1-deficient proerythroblast cells with erythrocyte differentiation potential
genotype/variation: expressing GATA1(D218Y)-ER
treated with: 100 nM estradiol for 24 hrs
Treatment protocol G1E cells expressing wild type or mutant versions of GATA1-ER were induced to differentiate for 24 hours with 100 nM estradiol.
Growth protocol G1E cells were cultured as described previously [PMID: 9032291].
Extracted molecule total RNA
Extraction protocol Trizol extraction of total RNA followed by purification via Qiagen RNeasy kit was performed according to the manufacturer's instructions.
Label biotin
Label protocol Affymetrix standard protocol. University of Pennsylvania Microarray Facillity.
 
Hybridization protocol Affymetrix standard protocol. University of Pennsylvania Microarray Facillity.
Scan protocol Affymetrix standard protocol. University of Pennsylvania Microarray Facillity.
Description D218Y_3
Data processing Affymetrix .CEL (probe intensity) files were imported into Partek Genomics Suite v6.6 where RMA normalization was performed yielding log2-transformed expression intensities for all transcript clusters on the array. RMA results were filtered to exclude control probesets. To find differentially expressed genes, a 1-way ANOVA was performed across the five conditions (each with three replicates) and all ten possible pairwise comparisons were performed, each yielding a p-value and a fold-change for all genes on the array. All p-values were corrected for False Discovery Rate (FDR) by the method of Benjamini and Hochberg as implemented in Partek. Genes with a p-value of less than 0.05 and a fold change more than or equal to 1.5 were used for further analysis. University of Pennsylvania Microarray Facillity.
 
Submission date Jan 08, 2013
Last update date Mar 05, 2013
Contact name Amy E. Campbell
E-mail(s) amy.e.campbell@cuanschutz.edu
Phone 303-724-1651
Organization name University of Colorado Anschutz Medical Campus
Street address 12801 E 17th Ave, Room L18-10403G
City Aurora
State/province CO
ZIP/Postal code 80045
Country USA
 
Platform ID GPL6246
Series (1)
GSE43356 Expression data from G1E erythroid cells expressing GATA1 mutants

Data table header descriptions
ID_REF
VALUE RMA processed and log2 transformed transcript-level signal

Data table
ID_REF VALUE
10421172 9.57939
10391649 6.71787
10481474 9.50526
10387505 9.70745
10348590 7.14359
10388194 9.44497
10351905 10.1634
10380773 9.19748
10539873 11.1639
10513608 11.6684
10460157 9.07352
10575534 9.47792
10384974 7.87779
10476252 8.28828
10445046 8.58455
10368199 11.5188
10396610 12.0842
10401891 9.08924
10582275 12.4659
10426557 10.778

Total number of rows: 28350

Table truncated, full table size 467 Kbytes.




Supplementary file Size Download File type/resource
GSM1060905_D218Y_3.CEL.gz 4.2 Mb (ftp)(http) CEL
Processed data included within Sample table

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