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Sample GSM711743 Query DataSets for GSM711743
Status Public on Jul 15, 2011
Title Drosophila_aly mutant testis_replicate 1
Sample type RNA
 
Source name aly mutant testis, replicate 1
Organism Drosophila melanogaster
Characteristics strain: aly2/aly5P mutant fly.
time point: 1 day old
Treatment protocol aly mutant testes were dissected in DEPC-treated 1× PBS buffer in 20 min interval, followed by immediate snap freezing in liquid nitrogen.
Growth protocol All fly stocks were grown in a 25 °C incubator with standard medium.
Extracted molecule total RNA
Extraction protocol Total RNA from approximately 200 pairs of fly testes was extracted using TRIzol (Invitrogen, #15596-018, Carlsbad, CA, USA) following the manufacturer's instructions. The genomic DNA was degraded using 2 Units of DNase I (Fermentas, #EN0521, Glen Burnie, MD, USA) at 37°C for 20 minutes. RNA integrity was checked by gel electrophoresis (1% agarose).
Label biotin
Label protocol Labeling was performed using Affymetrix's IVT labeling kit following manufacturer's directions.
 
Hybridization protocol Approximately 4 μg of total RNA from each biological replicate were used to generate labeling probes to hybridize with the Affymetix GeneChip Drosophila Genome 2.0 Array according to the Affymetrix protocol. Three biological replicates were performed for each genotype. Microarray hybridization was processed at the Core Facility at the Stanford University School of Medicine.
Scan protocol Scanning was performed with the Affymetrix GeneChip scanner using default settings.
Data processing The raw data were exported from the Affymetrix Microarray Suite (MAS). The CEL files were used for signal normalization with RMA as part of the limma package from the Bioconductor R packages (http://www.bioconductor.org).
 
Submission date Apr 19, 2011
Last update date Aug 28, 2018
Contact name Margaret T. Fuller
E-mail(s) [email protected]
Phone (650) 725-7681
Fax (650) 725-7739
URL http://cmgm.stanford.edu/~fullab/
Organization name Stanford University School of Medicine
Department Departments of Developmental Biology and Genetics
Lab Fuller Lab
Street address Beckman Center B300, 279 Campus Drive
City Stanford
State/province CA
ZIP/Postal code 94305-5329
Country USA
 
Platform ID GPL1322
Series (1)
GSE28728 Sequential changes at differentiation gene promoters as they become active in a stem cell lineage
Relations
Reanalyzed by GSE68696
Reanalyzed by GSM1933154
Reanalyzed by GSE119084

Data table header descriptions
ID_REF
VALUE RMA normalized signal intensity
ABS-CALL Absolute CALL, which indicates gene expression was present (P), absent (A) or marginal (M), was retrieved with the code of “eset” in the Affy package.

Data table
ID_REF VALUE ABS-CALL
1632993_at 20183.09 P
1633930_at 14014.45 P
1635424_s_at 10180.03 P
1633068_at 16267.95 P
1627235_at 3760.38 P
1628872_at 8363.86 P
1624444_at 7771.89 P
1631436_at 9318.03 P
1636364_a_at 3868.4 P
1624591_at 4960.16 P
1623978_at 6296.62 P
1624985_at 6740.75 P
1636039_at 6533.57 P
1630663_a_at 9651.22 P
1639413_at 8875.57 P
1636556_at 3606.78 P
1633212_s_at 11166.91 P
1632138_at 7615.69 P
1634343_at 7725.55 P
1623046_at 1716.71 P

Total number of rows: 18952

Table truncated, full table size 368 Kbytes.




Supplementary file Size Download File type/resource
GSM711743.CEL.gz 2.1 Mb (ftp)(http) CEL
Processed data included within Sample table

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