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Sample GSM320557 Query DataSets for GSM320557
Status Public on Sep 16, 2008
Title Chromosome 1 Replacement alpha-type Cell Replicate 2
Sample type genomic
 
Channel 1
Source name S. cerevisiae chromosome 1 replacement alpha-type cells
Organism Saccharomyces cerevisiae
Characteristics strain: W303;S. cerevisiae chromosome 1 was replaced by S. bayanus chromosome 1
Treatment protocol S. bayanus were crossed to S. cerevisiae to generate F1 hybrid cells. The hybrid diploids were induced to sporulate and viable spores were backcrossed to S. cerevisiae to construct chromosome replacement lines
Growth protocol Yeast cells were grown in YPD medium, at 30 degree
Extracted molecule genomic DNA
Extraction protocol Yeast genomic DNA was extracted using QIAGEN Genomic-tip 100/G kit
Label Cy5
Label protocol fragmentation protocol:4.5 µg total genomic DNA were digested by 1 µl Dnase I (0.05 U) at 37 degree for 5 minutes and at 100 degree, 15 minutes for enzyme inactivation. The label protocol was adapted from Microarray Core Facility, Insititute of Molecular Biology, Academia Sinica, TW (http://www.imb.sinica.edu.tw/mdarray/methods.html)
 
Channel 2
Source name S. cerevisiae alpha-type cells
Organism Saccharomyces cerevisiae
Characteristics strain: W303
Growth protocol Yeast cells were grown in YPD medium, at 30 degree
Extracted molecule genomic DNA
Extraction protocol Yeast genomic DNA was extracted using QIAGEN Genomic-tip 100/G kit
Label Cy3
Label protocol fragmentation protocol:4.5 µg total genomic DNA were digested by 1 µl Dnase I (0.05 U) at 37 degree for 5 minutes and at 100 degree, 15 minutes for enzyme inactivation. The label protocol was adapted from Microarray Core Facility, Insititute of Molecular Biology, Academia Sinica, TW (http://www.imb.sinica.edu.tw/mdarray/methods.html)
 
 
Hybridization protocol The hybridization protocol was adapted from Microarray Core Facility, Insititute of Molecular Biology, Academia Sinica, TW (http://www.imb.sinica.edu.tw/mdarray/methods.html)
Scan protocol Arrays were scanned for F635(cy5) and F532(Cy3) fluoresence intensities using AXON 4000B ( Molecular Device , sunnyvale , CA )
Description The S. cerevisiae hybrid karyotypes were analyzed by array-CGH to identify small regions of duplication or homeologous chromosomal exchange occurring during the strain construction.
Data processing Subtracted background. Dividing by ch2 (control) was used to transform data (Agilent GeneSpring 7.3.1 software)
 
Submission date Sep 15, 2008
Last update date Sep 15, 2008
Contact name Jun-Yi Leu
E-mail(s) jleu@imb.sinica.edu.tw
Organization name Academia Sinica
Department Insititute of Molecular Biolody
Street address 128 Academia Road, Section 2, Nankang
City Taipei
ZIP/Postal code 115
Country Taiwan
 
Platform ID GPL7305
Series (2)
GSE12776 Karyotype analysis of S. cerevisiae chromosome replacement lines - alpha-type cells
GSE12785 Karyotype analysis of S. cerevisiae chromosome replacement lines

Data table header descriptions
ID_REF
VALUE log ch1/ch2
ch1
ch2
RATIO ch1/ch2

Data table
ID_REF VALUE ch1 ch2 RATIO
1 -0.3002 42662 52530 0.8121454
2 -0.5929 7815 11787 0.6630186
3 -0.6857 23614 37984 0.6216828
4 -0.6353 13137 20405 0.6438128
5 -0.4115 23644 31448 0.7518443
6 -0.4059 23997 31793 0.7547888
7 -0.4749 15816 21981 0.7195305
8 -0.4983 23189 32756 0.7079314
9 -0.6157 21204 32491 0.6526115
10 -0.6568 13766 21703 0.6342902
11 -0.6047 30842 46901 0.6575979
12 -0.7622 10539 17875 0.5895944
13 -0.5455 7863 11476 0.68516904
14 -0.4451 14419 19630 0.734539
15 -0.4401 14229 19304 0.73710114
16 -0.4142 16710 22267 0.75043786
17 -0.3671 14938 19267 0.7753153
18 -0.3370 38051 48064 0.7916736
19 -0.5779 10443 15588 0.6699384
20 -0.5935 16193 24434 0.6627241

Total number of rows: 6400

Table truncated, full table size 199 Kbytes.




Supplementary data files not provided
Processed data included within Sample table

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