NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM1513367 Query DataSets for GSM1513367
Status Public on Jun 26, 2015
Title E18 Ctx total 18A
Sample type RNA
 
Source name Cortex
Organism Mus musculus
Characteristics developmental stage: E18
Treatment protocol There were no specific treatments of the animals prior to collection.
Growth protocol Timed pregnant dams were collected at the times indicated. Mice were wild-type CD-1 from Charles River.
Extracted molecule total RNA
Extraction protocol Total cellular RNA was made from frozen tissue samples using standard Trizol protocols.
Label biotin
Label protocol Single-stranded cDNA was generated from the amplified cRNA with the WT cDNA Synthesis Kit (Affymetrix) and then fragmented and labeled with the WT Terminal Labeling Kit (Affymetrix).
 
Hybridization protocol Samples were hybridized with GeneChip Human Exon 1.0 ST Arrays (Affymetrix) and scanned at the UCLA Microarray Core Facility.
Scan protocol Array scanning was performed according to the manufacturer's instruction (Affymetrix)
Description RMA expression value derived from Expression Console software; core-exon analysis
Data processing Raw data were processed with the Exon Array Computational Tool (ExACT) (Affymetrix) for background correction and normalization. Data analysis and statistical evaluations were performed with customized R codes (version 2.3.1, http://www.r-project.org/). We defined a probeset as present when it had a P value <0.001 and an Intensity value >200. These criteria were suggested by the results of preliminary experiments. The SECT includes all probesets present in at least 16 of the 18 arrays. In addition, we refined the SECT to remove GC-rich (i.e., >=80%) probesets. The concordance between the SECT and the normal salivary core transcriptome (NSCT) was evaluated assuming hypergeometric distributions.
 
Submission date Sep 25, 2014
Last update date Jun 26, 2015
Contact name Ronald P. Hart
E-mail(s) [email protected]
Phone 848-445-1783
Organization name Rutgers University
Department Cell Biology & Neuroscience
Street address 604 Allison Rd Rm B430
City Piscataway
State/province NJ
ZIP/Postal code 08854
Country USA
 
Platform ID GPL6096
Series (1)
GSE61751 Microarray analysis of developing mouse cortex reveals regulation of ribosomal protein mRNAs throughout development

Data table header descriptions
ID_REF
VALUE Quantification

Data table
ID_REF VALUE
6848511 10.3952
6864895 7.67426
6766590 3.88011
6914045 4.67053
6963197 6.48859
6766588 4.16723
6995964 7.49421
6766587 5.9065
6815739 8.35839
6766586 9.87708
7012346 6.03988
6766585 7.07359
6848505 6.52401
6766584 5.4364
6848504 6.74627
6979576 5.88249
6995960 11.8843
6766583 5.2952
6963191 7.09973
6979575 6.89042

Total number of rows: 23332

Table truncated, full table size 362 Kbytes.




Supplementary file Size Download File type/resource
GSM1513367_E18_ctx_total_18A_ctx.CEL.gz 25.1 Mb (ftp)(http) CEL
GSM1513367_E18_ctx_total_18A_ctx.rma.rma-gene-core.chp.gz 172.3 Kb (ftp)(http) CHP
Processed data included within Sample table

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