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Sample GSM189559 Query DataSets for GSM189559
Status Public on May 17, 2007
Title Fig 1AB: wt (A11311) batch RNA 4
Sample type RNA
 
Channel 1
Source name 11311 set#6 RNA
Organism Saccharomyces cerevisiae
Characteristics Strain Name : wt (A11311)
Biomaterial provider Cheryl Christianson, Dunham Lab, Princeton University
Extracted molecule total RNA
Extraction protocol Description : Filters were incubated for 1 hour at 65oC in lysis buffer (10 mM EDTA, 0.5% SDS, and 10 mM Tris, pH 7.5) and acid phenol. The aqueous phase was further extracted twice with an equal volume of chloroform using phase lock gel (Eppendorf). Total RNA was then ethanol precipitated and further purified over RNeasy columns (Qiagen). RNA quality was checked using the Bioanalyzer RNA Nano kit.
Label Cy3
Label protocol Description : 325 ng was used for microarray labeling with the Agilent Low RNA Input Fluorescent Linear Amplification Kit. Reactions were performed as directed except using half the recommended reaction volume and one quarter the recommended Cy-CTP amount. Dye incorporation and yield were measured with a Nanodrop spectrophotometer.
 
Channel 2
Source name 11311 set#5 RNA
Organism Saccharomyces cerevisiae
Characteristics Strain Name : wt (A11311)
Biomaterial provider Cheryl Christianson, Dunham Lab, Princeton University
Growth protocol Description : Cultures were grown overnight at 30C in selective -his/G418 media and then diluted back to OD=0.3 in 250 ml -his/G418 media. Cultures were grown shaking at 30C to midlog (OD=1.0-1.3) and harvested by vacuum filtration, flash-frozen in liquid nitrogen, and stored at ?80oC until RNA extraction.
Extracted molecule total RNA
Extraction protocol Description : Filters were incubated for 1 hour at 65oC in lysis buffer (10 mM EDTA, 0.5% SDS, and 10 mM Tris, pH 7.5) and acid phenol. The aqueous phase was further extracted twice with an equal volume of chloroform using phase lock gel (Eppendorf). Total RNA was then ethanol precipitated and further purified over RNeasy columns (Qiagen). RNA quality was checked using the Bioanalyzer RNA Nano kit.
Label Cy5
Label protocol Description : 325 ng was used for microarray labeling with the Agilent Low RNA Input Fluorescent Linear Amplification Kit. Reactions were performed as directed except using half the recommended reaction volume and one quarter the recommended Cy-CTP amount. Dye incorporation and yield were measured with a Nanodrop spectrophotometer.
 
 
Hybridization protocol Description : Equal masses of differentially labeled control and sample cRNA were combined such that each sample contained at least 2.5 pmol dye. Samples were mixed with control targets, fragmented, combined with hybridization buffer, and applied to a microarray consisting of 60mer probes for each yeast open reading frame (Agilent). Microarrays were rotated at 60?C for 17 hours in a hybridization oven (Agilent). Arrays were then washed according to the Agilent SSPE wash protocol, and scanned on an Agilent scanner.
Scan protocol Pixel Size : 10
Scan Date : 2006-01-31
Scan Time : 11:37:52
Scanner Make : Agilent Technologies Scanner
Scanner Model : G2505B
Scanning software : ChipScan
Scanning software version : A.6.3.1
Description former name: AA 11311 set#5 vs. 11311 set#6 batch RNA
Data processing Extraction Software : Agilent Feature Extractor
Extraction Software Version : A.7.5.1
Datafile type : Agilent result file
 
Submission date May 15, 2007
Last update date May 16, 2007
Contact name Maitreya J. Dunham
E-mail(s) maitreya@uw.edu
Phone 206-543-2338
Organization name University of Washington
Department Genome Sciences
Lab Dunham Lab
Street address Foege Building, S403B, Box 355065
City Seattle
State/province WA
ZIP/Postal code 98195-5065
Country USA
 
Platform ID GPL2883
Series (1)
GSE7812 Effects of aneuploidy on cellular physiology and cell division in haploid yeast.

Data table header descriptions
ID_REF Uniquely identifies feature/spot in array layout.
VALUE log(base 2) (R_PROCESSED_SIGNAL/G_PROCESSED_SIGNAL)
R_PROCESSED_SIGNAL The propagated feature signal in the red channel, used for computation of log ratio
G_PROCESSED_SIGNAL The propagated feature signal in the green channel, used for computation of log ratio
R_MEAN_SIGNAL Mean foreground intensity Ch 2.
G_MEAN_SIGNAL Mean foreground intensity Ch 1.

Data table
ID_REF VALUE R_PROCESSED_SIGNAL G_PROCESSED_SIGNAL R_MEAN_SIGNAL G_MEAN_SIGNAL
1 -6.644 51.76124 70475.9 36.67241 5172.966
2 0 27.58976 34.79775 25.4386 27.24561
3 -.505 1416.735 2010.899 294.1429 172.3214
4 -.22 450.8489 524.9925 113.069 63.62069
5 -.149 2643.518 2930.481 519.8276 241.7586
6 .048 47.15942 45.60957 35.61404 29.2807
7 -1.033 28.39992 58.12154 32.15625 30.25
8 .48 796.6059 571.0256 178.6129 67.06452
9 -.222 1803.186 2102.901 366 179.5
10 -.238 8401.485 9906.2 1586 759.1333
11 -.211 669.931 775.6024 154.4737 81.85965
12 -.278 3037.555 3682.426 591.9655 297.8276
13 .176 101.8611 90.17471 46.32787 32.40984
14 .006 16667.9 16599.06 3127.65 1251.517
15 0 29.8968 40.28782 32.39683 27.93651
16 .163 2490.841 2225.04 493.2414 189.1724
17 0 21.25588 40.51389 29.10526 28.03509
18 .021 9621.097 9484.835 1812.456 727.9298
19 -.118 19527.62 21197.98 3666.246 1588.263
20 0 28.80565 45.16995 32.22951 28.01639

Total number of rows: 10789

Table truncated, full table size 476 Kbytes.




Supplementary file Size Download File type/resource
GSM189559.txt.gz 2.4 Mb (ftp)(http) TXT
Processed data included within Sample table

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