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Sample GSM413966 Query DataSets for GSM413966
Status Public on Jun 18, 2009
Title DAMC233 array
Sample type genomic
 
Channel 1
Source name DAMC233 chromosomal DNA labeled with Cy5
Organism Saccharomyces cerevisiae
Characteristics strain: DAMC233
ploidy: diploid
recombination: illegitimate
Extracted molecule genomic DNA
Extraction protocol Genomic DNA was harvested by standard protocol: Cells were treated with zymolyase to obtain spheroblasts. SDS was used to disrupt the cell membrane. Potassium acetate was used to precipitate protein and lipids. DNA was precipitated with isopropanol. RNAse A was used to degrade RNA.
Label Cy5
Label protocol Direct incorporation with klenow polymerase and random priming
 
Channel 2
Source name MS71 chromosomal DNA labeled with Cy3
Organism Saccharomyces cerevisiae
Characteristics strain: MS71
isogenicity: isogenic to the strain in Channel 1
Extracted molecule genomic DNA
Extraction protocol Genomic DNA was harvested by standard protocol: Cells were treated with zymolyase to obtain spheroblasts. SDS was used to disrupt the cell membrane. Potassium acetate was used to precipitate protein and lipids. DNA was precipitated with isopropanol. RNAse A was used to degrade RNA.
Label Cy3
Label protocol Direct incorporation with klenow polymerase and random priming
 
 
Hybridization protocol Described in Lemoine, F. et al. Cell, Vol. 120, 587-598 (2005).
Scan protocol Array scanned in Genepix 4000b scanner.
Description DAMC233 is an illegitimate diploid from a mating between an mre11-H125N mutant version of the GAL-POL1 strain described in Lemoine, F. et al. Cell, Vol. 120, 587-598 (2005) and the test mater 1225alpha (also described in Lemoine et al.). Genomic DNA from DAMC233 was competitively hybridized with genomic DNA from the isogenic reference strain MS71. This experiment allows the determination of chromosomal rearrangements in DAMC233.
Data processing The log2 R/G ratios for all probes in the array were collapsed to a single value in the case of repeated probes and normalized according to the median value for the entire array.
 
Submission date Jun 06, 2009
Last update date Jun 17, 2009
Contact name Anne Casper
E-mail(s) [email protected]
Phone (919) 684-5891
Organization name Duke University
Department Department of Molecular Genetics and Microbiology
Lab Laboratory of T. Petes
Street address 381 CARL Building, Research Drive, Box 3054
City Durham
State/province NC
ZIP/Postal code 27710
Country USA
 
Platform ID GPL4414
Series (1)
GSE16502 Analysis of genome rearrangements in S. cerevisiae strains with low levels of DNA polymerase alpha

Data table header descriptions
ID_REF
VALUE Log2 Red (DAMC233)/Green (MS71) ratio

Data table
ID_REF VALUE
302 -0.31
303 0.3
304 -0.11
305 -0.07
306 0.3
307 -0.32
308 -0.22
309 0.18
310 0.17
311 0.3
312 0.2
313 0.35
314 -0.05
315 0.03
316 -0.25
317 -0.65
318 -0.04
319 -0.06
320 -0.02
321 -0.23

Total number of rows: 13100

Table truncated, full table size 136 Kbytes.




Supplementary file Size Download File type/resource
GSM413966.gpr.gz 1.7 Mb (ftp)(http) GPR
Processed data included within Sample table

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