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Sample GSM255869 Query DataSets for GSM255869
Status Public on Feb 04, 2008
Title YAP4-TAP 7.1mM MMS treatment replicate 1
Sample type genomic
 
Channel 1
Source name YAP4-TAP, 7.1mM MMS, input DNA
Organism Saccharomyces cerevisiae
Characteristics Yeast BY4741 strain with YAP4-TAP
Extracted molecule genomic DNA
Extraction protocol Cells were fixed with 1% formaldehyde, lysed, and sonicated to shear DNA. DNA fragments bound by the tagged TF were enriched by immunoprecipitation with an anti-TAP antibody (Open Biosystems). Afer reversal of crosslinking, DNA fragments were purified by phenol chloroform extraction
Label Cy3
Label protocol non-antibody enriched DNA sample was amplified by LM-PCR using a Cy3 label.
 
Channel 2
Source name YAP4-TAP, 7.1mM MMS, anti-TAP enriched
Organism Saccharomyces cerevisiae
Characteristics Yeast BY4741 strain with YAP4-TAP
Extracted molecule genomic DNA
Extraction protocol Cells were fixed with 1% formaldehyde, lysed, and sonicated to shear DNA. DNA fragments bound by the tagged TF were enriched by immunoprecipitation with an anti-TAP antibody (Open Biosystems). Afer reversal of crosslinking, DNA fragments were purified by phenol chloroform extraction
Label Cy5
Label protocol Enriched DNA was amplified and Cy5-labeled by ligation-mediated PCR (LM-PCR).
 
 
Hybridization protocol Cy-3 and Cy-5 labeled samples were mixed with hybridization buffer (Agilent In Situ Hybridization Kit) and co-hybridized to the Yeast Whole Genome Tiling Array (G4486A, Agilent Technologies). Slides were hybridized for 17h at 60 degree Celcius in a rotating oven, and washed
Scan protocol Scanned on an GenePix 4000A scanner (Axon Instruments) at a 10.0 um resolution
Images were quantified using GenePix Pro 6.0 software (Axon Instruments)
Description yeast cells treated with 7.1mM MMS, enriched DNA compared to input genoimc DNA.
Data processing Background subtraction. Background-adjusted log ratios were then corrected for cyanine-dye dependent bias using Loess normalization
 
Submission date Jan 10, 2008
Last update date Feb 04, 2008
Contact name Kai Tan
Organization name University of California San Diego
Department Bioengineering
Street address 9500 Gilman Drive
City La Jolla
State/province CA
ZIP/Postal code 92093
Country USA
 
Platform ID GPL3737
Series (1)
GSE10146 A systems approach to delineate functions of YAP family members

Data table header descriptions
ID_REF
VALUE log10(Cy5signal/Cy3signal) per feature (normalized signals used)
CH1_SIG_MEAN mean normalized foreground signal from Cy3 channel
CH2_SIG_MEAN mean normalized foreground signal from Cy5 channel

Data table
ID_REF VALUE CH1_SIG_MEAN CH2_SIG_MEAN
29990 2.1158 3 390.5
27136 2.0636 2.9 332.7
24580 2.0553 2.1 240.6
33449 1.9818 4.3 413.8
39904 1.8896 14.3 1110.9
40993 1.7104 1.2 60.5
11010 1.6108 22.5 919.8
13562 1.5942 44.3 1739.2
43531 1.5937 73.4 2878.9
2840 1.5926 69.4 2716.7
39661 1.5905 2.4 93.5
6181 1.543 22.4 780.9
6743 1.5303 798.6 27081.4
40180 1.5153 4.7 155.4
40785 1.5109 2 64.6
22731 1.4847 5 152.6
38946 1.4641 51 1484.8
17972 1.4572 16 459.2
17268 1.4412 917.2 25329.8
10158 1.422 3.2 83.9

Total number of rows: 44290

Table truncated, full table size 1099 Kbytes.




Supplementary file Size Download File type/resource
GSM255869.gpr.gz 6.1 Mb (ftp)(http) GPR
Processed data included within Sample table

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