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Sample GSM1124845 Query DataSets for GSM1124845
Status Public on May 14, 2018
Title Sfpq heterologous knock-out 1
Sample type RNA
 
Source name Sfpq+/- (Sfpq heterologous knock-out)
Organism Mus musculus
Characteristics developmental stage: embryo
age: E13.5
tissue: brain (cerebral cortical region)
genotype/variation: Sfpq+/-
Growth protocol Embryonic cerebral cortices were disected, isoalted in eppendorf tube, and quickly frozen in Liquid nitrogen.
Extracted molecule total RNA
Extraction protocol Total RNA from cerebral cortical regions of control, Sfpq+/-,and Sfpq+/- brains were extracted using Rneasy Plus Micro (Qiagen) according to the manufacturer’s instructions.
Label biotin
Label protocol Single-stranded cDNA was generated from the amplified cRNA with the WT Expression Kit (Ambion) and then fragmented and labeled with the WT Terminal Labelingand and Controls Kit (Affymetrix).
 
Hybridization protocol Samples were hybridized with GeneChip Mouse Exon 1.0 ST Arrays (Affymetrix) and scanned.
Scan protocol Array scanning was performed according to the manufacturer's instruction (Affymetrix)
Description RNA expression value derived from Expression Console software; full-exon analysis
Data processing RNA expression value derived from Expression Console software; full-exon analysis
Raw data were processed with the Expression Console 1.2.0.20 (Affymetrix) for background correction and normalization. Data analysis and statistical evaluations were performed according to our previous plublication (Yamashita et al. J. Hum. Genet. 57, 368-374). )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 Apr 17, 2013
Last update date May 14, 2018
Contact name Mikako Ito
E-mail(s) ito@med.nagoya-u.ac.jp
Organization name Nagoya University Graduate School of Medicine
Lab Neurogenetics
Street address 65 Tsurumai, Showa-ku
City Nagoya
ZIP/Postal code 4668550
Country Japan
 
Platform ID GPL6193
Series (1)
GSE46138 Exon Level Expression Profiling: a Novel Unbiased Transcriptome

Data table header descriptions
ID_REF
VALUE Quantification
DETECTION P-VALUE

Data table
ID_REF VALUE DETECTION P-VALUE
4304920 2.14993 0.808988
4304921 2.54419 0.829153
4304922 6.5566 9.92264e-05
4304923 7.03329 6.11096e-05
4304925 8.10027 3.00684e-06
4304927 3.7111 0.492829
4304928 10.7023 2.98754e-08
4304929 12.4608 1.88799e-08
4304930 4.62093 0.00942263
4304931 4.36798 0.0313138
4304932 4.55325 0.0186833
4304933 2.82063 0.238968
4304934 3.91183 0.136731
4304935 4.57408 0.117137
4304937 8.08479 1.71286e-06
4304938 8.57823 1.47389e-06
4304939 2.12592 0.30703
4304940 5.13097 0.149154
4304941 5.78751 0.0257739
4304942 9.16887 0.00230673

Total number of rows: 1256831

Table truncated, full table size 31819 Kbytes.




Supplementary file Size Download File type/resource
GSM1124845_1.Het1.CEL.gz 23.9 Mb (ftp)(http) CEL
GSM1124845_1.Het1.rma-exon-all-dabg.chp.gz 11.7 Mb (ftp)(http) CHP
Processed data included within Sample table
Processed data provided as supplementary file

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