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Sample GSM320578 Query DataSets for GSM320578
Status Public on Sep 16, 2008
Title Chromosome 7 Replacement alpha-type Cell Replicate 2
Sample type genomic
 
Channel 1
Source name S. cerevisiae chromosome 7 replacement alpha-type cells
Organism Saccharomyces cerevisiae
Characteristics strain: W303;S. cerevisiae chromosome 7 was replaced by S. bayanus chromosome 7
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 -0.2097 32205 37244 0.86470306
2 -0.4329 9656 13035 0.7407748
3 -0.4367 21722 29401 0.7388184
4 -0.3486 18613 23701 0.7853255
5 -0.3309 23672 29774 0.7950561
6 -0.2879 23629 28847 0.8191146
7 -0.2616 18936 22701 0.8341483
8 -0.3619 26040 33465 0.7781264
9 -0.3337 21838 27522 0.7934743
10 -0.4087 15376 20412 0.75328237
11 -0.3658 28464 36679 0.7760299
12 -0.4219 8302 11122 0.74644846
13 -0.4077 8590 11395 0.7538394
14 -0.2700 20618 24862 0.8292977
15 -0.2401 17516 20687 0.84671533
16 -0.2372 21009 24763 0.84840286
17 -0.2120 21017 24344 0.8633339
18 0.0317 43692 42742 1.0222263
19 -0.3389 14398 18211 0.79062104
20 -0.2366 20742 24439 0.8487254

Total number of rows: 6400

Table truncated, full table size 202 Kbytes.




Supplementary data files not provided
Processed data included within Sample table

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