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Sample GSM701879 Query DataSets for GSM701879
Status Public on Nov 30, 2011
Title brain_dove Ac_rep2
Sample type RNA
 
Source name Ac dove
Organism Streptopelia risoria
Characteristics brain area: surrounding arcopallium
gender: Male
age: Adult
Extracted molecule total RNA
Extraction protocol After laser capture the samples, the cap membrane with nuclei were carefully removed and placed in a 0.65 ml tube of the PicoPure RNA isolation kit which contained 50ul of disruption buffer (Molecular Devices). Tubes were placed on a 42oC heat block for 30 min then placed in a -80 oC freezer until all desired samples were captured. Total RNA was then isolated according to the remaining protocol steps in the PicoPure isolation kit instructions (Molecular Devices). The concentration and integrity of total RNA were measured on a 2100 Bioanalyzer (Agilent Technologies, Santa Clara, CA USA) using the RNA Pico 6000 kit according to manufacturer instructions (Agilent Technologies).
Label Cy3
Label protocol Samples were labeled with Cy3-dCTP using the uMACS SuperAmp Kit (Miltenyi Biotec).
 
Hybridization protocol From the amplified cDNA reactions, 1.5 mg of amplified labeled product (probe) was denatured and hybridized to our custom designed songbird oligo spotted arrays (Agilent Technologies; Whitney et al, in preparation) containing oligos designed from over 44,000 relatively unique cDNA transcripts, including some splice variants. More detailed information on the arrays is available at http://aviangenomes.org/main/zebrafincholigoarray.
Scan protocol After hybridization, the microarrays were scanned with the Axon GenePix 4000B scanner to acquire and analyze the expression data (Molecular Devices).
Description gene expression brain
Data processing For analysis, signal intensity on an axon array scanner was obtained in Agilent oligoarray format. The data was extracted in R using the Agi4x44PreProcess Bioconductor library.The values were normalized using median centered log2 transformation. Raw and normalized expression distributions were evaluated for sample quality control using the normalization centering profile, the normalization factor, and a cross-sample correlation analysis. Normalization was evaluated with VSN (variance stabilization normalization)-Scale Factor package in R (R Foundation for Statistical Computing, Vienna, Austria). VSN-Scale Factor was chosen because it performed the least manipulation of the original intensity profiles, and normalizes samples among themselves.
 
Submission date Apr 05, 2011
Last update date Nov 30, 2011
Contact name Erina Hara
Organization name Duke University Medical Center
Street address Rm 449 Bryan Research Building
City Durham
State/province NC
ZIP/Postal code 27710
Country USA
 
Platform ID GPL9856
Series (1)
GSE28395 Avian arcopallium

Data table header descriptions
ID_REF
VALUE Normalized log2 transformation

Data table
ID_REF VALUE
0205P0030B17 212
0202P0024M14 532
0205P0028D09 156
0202P0019C06 184
0203P0050F15 413
0206P0012J11 169
0203P0070P07 163
0202P0043B09 147
0106P0001D01 264
0203P0043A22 155
0206P0018B06 400
0202P0038K07 3444
0206P0020E24 215
0057P0001C12 48312
0106P0009G08 292
0202P0008C24 347
0203P0022P10 164
0206P0021I07 198
0106P0001B01 199
0063P0031D01 199

Total number of rows: 43125

Table truncated, full table size 726 Kbytes.




Supplementary file Size Download File type/resource
GSM701879_2317_4964_CU_074_AgilentSongbird2_47_GE1-v5_95_Feb07_1_4.txt.gz 6.4 Mb (ftp)(http) TXT
Processed data included within Sample table

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