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Sample GSM320581 Query DataSets for GSM320581
Status Public on Sep 16, 2008
Title Chromosome 9 Replacement alpha-type Cell Replicate 1
Sample type genomic
 
Channel 1
Source name S. cerevisiae chromosome 9 replacement alpha-type cells
Organism Saccharomyces cerevisiae
Characteristics strain: W303;S. cerevisiae chromosome 9 was replaced by S. bayanus chromosome 9
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 -0.0602 26514 27644 0.95912313
2 -0.1609 7019 7847 0.89448196
3 -0.2579 15792 18883 0.83630776
4 -0.1733 15040 16960 0.8867925
5 -0.1064 17572 18917 0.92889994
6 -0.0948 20369 21753 0.9363766
7 -0.1027 11899 12777 0.93128276
8 -0.2528 19585 23336 0.83926123
9 -0.1818 14613 16576 0.88157576
10 -0.2934 12608 15451 0.815999
11 -0.3439 21756 27613 0.7878898
12 -0.2941 9763 11971 0.81555426
13 0.0025 6868 6856 1.0017503
14 -0.1370 15920 17506 0.9094025
15 -0.0126 11941 12046 0.9912834
16 -0.1266 15882 17339 0.9159698
17 0.0431 12065 11710 1.030316
18 0.0246 35814 35209 1.0171831
19 -0.0611 8320 8680 0.95852536
20 -0.1263 15416 16827 0.9161467

Total number of rows: 6400

Table truncated, full table size 204 Kbytes.




Supplementary data files not provided
Processed data included within Sample table

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