NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM189562 Query DataSets for GSM189562
Status Public on May 17, 2007
Title Fig 1AB: Dis XIV (A13979) batch RNA 2
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 13979 set#6 RNA
Organism Saccharomyces cerevisiae
Characteristics Strain Name : Dis XIV (A13979)
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 : 10:39:38
Scanner Make : Agilent Technologies Scanner
Scanner Model : G2505B
Scanning software : ChipScan
Scanning software version : A.6.3.1
Description former name: AA chr 14 disome (13979) 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 54.10845 77667 37.1129 5549.065
2 0 27.39555 26.31627 26.24561 24.84211
3 -.014 2204.845 2226.073 468.2742 181.9677
4 -.044 556.748 573.9781 140.5439 63.07018
5 -.221 2820.611 3288.307 585.8246 260.2807
6 .114 72.72508 67.18175 40.77966 27.86441
7 -.816 36.8167 64.81172 33.51667 27.8
8 -.082 595.6053 630.3455 148.6333 66.95
9 -.506 1577.604 2240.489 344.9615 181.7885
10 -.163 10059.77 11262.29 1983.911 851.3036
11 -.367 672.8781 867.919 164.6316 83.4386
12 -.294 3260.374 3998.034 671.1034 312.3276
13 .754 124.1784 73.62273 51.48214 28.14286
14 .45 22099.83 16176.91 4229.435 1240.258
15 -.85 28.23586 50.88223 31.89286 26.71429
16 .305 3085.388 2497.087 640.0862 202.569
17 0 22.6587 35.05431 30.19643 23.89286
18 -.137 7631.71 8389.523 1523.644 634.8983
19 -.556 15836.34 23289.61 3036.148 1776.705
20 -.506 42.24341 59.99157 34.83333 27.2037

Total number of rows: 10789

Table truncated, full table size 476 Kbytes.




Supplementary file Size Download File type/resource
GSM189562.txt.gz 2.4 Mb (ftp)(http) TXT
Processed data included within Sample table

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