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Sample GSM1880728 Query DataSets for GSM1880728
Status Public on Mar 14, 2018
Title Mesocosm growth, day 7, Replicate 2
Sample type RNA
 
Channel 1
Source name mycelia, drought, day 7
Organism Agaricus bisporus
Characteristics strain: var bisporus (H97)
tissue: mycelia
stress: drought
treatment: none
Treatment protocol Drought treatment was applied by stopping irrigation; samples were taken after 3 and 7 days, respectively;
Growth protocol Agaricus bisporus hyphae on agar medium were placed on hay in gas-tight mesocosms and irrigated for three weeks with water or water containing 50 µM Riboflavin;
Extracted molecule total RNA
Extraction protocol Total RNA was extracted using the Rneasy Microarray Tissue Kit (Qiagen GmbH, Hilden, Germany);
Label Cy5
Label protocol RNA was labelled using the Low Input Quick Amp Labeling Kit (Agilent Technologies, Santa Clara, CA, USA);
 
Channel 2
Source name mycelia, irrigated, day 7
Organism Agaricus bisporus
Characteristics strain: var bisporus (H97)
tissue: mycelia
stress: irrigated
treatment: none
Treatment protocol Drought treatment was applied by stopping irrigation; samples were taken after 3 and 7 days, respectively;
Growth protocol Agaricus bisporus hyphae on agar medium were placed on hay in gas-tight mesocosms and irrigated for three weeks with water or water containing 50 µM Riboflavin;
Extracted molecule total RNA
Extraction protocol Total RNA was extracted using the Rneasy Microarray Tissue Kit (Qiagen GmbH, Hilden, Germany);
Label Cy3
Label protocol RNA was labelled using the Low Input Quick Amp Labeling Kit (Agilent Technologies, Santa Clara, CA, USA);
 
 
Hybridization protocol Hybridization and washing if the Microarrays was perfomed as described in the Low Input Quick Amp Labeling Kit (Agilent Technologies)
Scan protocol Microarrays were scanned using a high-resolution scanner G2505C (Agilent Technologies) and Agilent's Feature Extraction software (v. 11.5.1.1) was used to quantify hybridization signals;
Description Biological replicate 1 of 2, harvest day 7, dye-swap
Data processing Data were processed using LIMMA: background correction (normexp), normalized within arrays (loess), normalized between arrays (Aquantile);
 
Submission date Sep 14, 2015
Last update date Mar 14, 2018
Contact name Alfons R Weig
E-mail(s) a.weig@uni-bayreuth.de
Organization name University of Bayreuth
Department Genomics and Bioinformatics
Street address Universitaetsstrasse 30
City Bayreuth
ZIP/Postal code 95447
Country Germany
 
Platform ID GPL20913
Series (1)
GSE73010 Vitamin B2 and drought stress responses in Agaricus bisporus

Data table header descriptions
ID_REF
VALUE normalized (loess and Aquantile) log2 values;

Data table
ID_REF VALUE
1 0.268769983
2 0.021819488
3 -0.112326184
4 -0.265115122
5 -0.258819251
6 -0.410685097
7 0.118685955
8 -0.527098665
9 -0.462922944
10 -0.42391986
11 -0.132969993
12 -0.269800298
13 -0.314506741
14 -0.128125078
15 -0.480379967
16 -0.073069183
17 -0.348171706
18 -0.38778562
19 -0.263831519
20 -0.120247669

Total number of rows: 15744

Table truncated, full table size 272 Kbytes.




Supplementary file Size Download File type/resource
GSM1880728_071199_1_4.txt.gz 1.2 Mb (ftp)(http) TXT
Processed data included within Sample table

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