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Sample GSM991848 Query DataSets for GSM991848
Status Public on Mar 31, 2013
Title sml1.UT vs. sml1.MMS, rep2
Sample type RNA
 
Channel 1
Source name sml1, MMS
Organism Saccharomyces cerevisiae
Characteristics genetic background: BY4741
genotype/variation: sml1Δ
treatment: methyl methanesulfonate (MMS)
Treatment protocol Conditions are untreated (UT) or methyl methanesulfonate (MMS-0.033%) treated.
Growth protocol For these experiments, 100 ml cultures for each strain were grown to an OD600 density of 0.8-1.0 at 30oC, split into two 50 ml cultures, and incubated for one additional hour either in the presence (MMS-treated) or absence (untreated) of 0.03% MMS (methyl methanesulfonate; Sigma 129925).
Extracted molecule total RNA
Extraction protocol RNA was isolated by hot phenol/chloroform extraction and enriched for mRNA via the Poly(A) Purist Kit (Ambion AM1916, Austin, TX, USA).
Label Cy3
Label protocol As described in Kuo D, Tan K, Zinman G, Ravasi T, Bar-Joseph Z, Ideker T (2010) Evolutionary divergence in the fungal response to fluconazole revealed by soft clustering. Genome Biol 11: R77 (PMID 20653936).
 
Channel 2
Source name sml1, untreated
Organism Saccharomyces cerevisiae
Characteristics genetic background: BY4741
genotype/variation: sml1Δ
treatment: none
Treatment protocol Conditions are untreated (UT) or methyl methanesulfonate (MMS-0.033%) treated.
Growth protocol For these experiments, 100 ml cultures for each strain were grown to an OD600 density of 0.8-1.0 at 30oC, split into two 50 ml cultures, and incubated for one additional hour either in the presence (MMS-treated) or absence (untreated) of 0.03% MMS (methyl methanesulfonate; Sigma 129925).
Extracted molecule total RNA
Extraction protocol RNA was isolated by hot phenol/chloroform extraction and enriched for mRNA via the Poly(A) Purist Kit (Ambion AM1916, Austin, TX, USA).
Label Cy5
Label protocol As described in Kuo D, Tan K, Zinman G, Ravasi T, Bar-Joseph Z, Ideker T (2010) Evolutionary divergence in the fungal response to fluconazole revealed by soft clustering. Genome Biol 11: R77 (PMID 20653936).
 
 
Hybridization protocol According to the protocol recommended by Agilent.
Scan protocol GenePix 4000A Scanner, Quantitation w/ GenePix 6.0.
Description US22502657_251507211176_S01_H_flip_3-4.avg
Data processing Lowess normalized, quantile normalized, LIMMA model.
 
Submission date Aug 23, 2012
Last update date May 07, 2013
Contact name Eric Jaehnig
E-mail(s) ejaehnig@ucsd.edu
Organization name Ludwig Institute for Cancer Research
Department Laboratory of Cancer Genetics
Lab Kolodner
Street address 9500 Gilman Dr
City La Jolla
State/province CA
ZIP/Postal code 92093
Country USA
 
Platform ID GPL9294
Series (1)
GSE40351 DNA damage checkpoint kinases regulate a global network of transcription factors

Data table header descriptions
ID_REF
VALUE Lowess- and quantile-normalized log2 ratio (MMS/UT)

Data table
ID_REF VALUE
A_06_P1519 0.389614275
A_06_P5727 0.231346923
A_06_P5667 -0.287372147
A_06_P1931 0.175520004
A_06_P2126 -0.102055613
A_06_P5610 -0.463895686
A_06_P3723 -0.060731394
A_06_P1675 0.087091276
A_06_P1087 -0.110577188
A_06_P6568 0.331796883
A_06_P7046 -0.045142849
A_06_P5705 0.453939773
A_06_P3628 0.210645511
A_06_P4724 0.088133055
A_06_P6190 -0.065171449
A_06_P4910 0.195393956
A_06_P2545 0.156395332
A_06_P3168 -0.297289535
A_06_P4543 -0.055524438
A_06_P4487 -0.388998438

Total number of rows: 6269

Table truncated, full table size 143 Kbytes.




Supplementary file Size Download File type/resource
GSM991848_US22502657_251507211176_S01_H_flip_3-4.avg.gpr.gz 796.8 Kb (ftp)(http) GPR
Processed data included within Sample table

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