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Sample GSM1636253 Query DataSets for GSM1636253
Status Public on Mar 20, 2015
Title Com2_T+1.5
Sample type RNA
 
Channel 1
Source name reference
Organism Bacillus subtilis
Characteristics strain: PY79
Extracted molecule total RNA
Extraction protocol RNA was extracted using the Hot Phenol method followed by Dnase treatment and cleaning with Qiagen's Rneasy kit
Label cy3
Label protocol 6-10 ug of RNA was labelled using Agilent's Fairplay III Protocol for NHS-ester dye-coupling reaction to amino allyl dUTP . Cy3 and Cy5 were purchased from GE Healthcare
 
Channel 2
Source name sample
Organism Bacillus subtilis
Characteristics strain: PY79
Extracted molecule total RNA
Extraction protocol RNA was extracted using the Hot Phenol method followed by Dnase treatment and cleaning with Qiagen's Rneasy kit
Label cy5
Label protocol 6-10 ug of RNA was labelled using Agilent's Fairplay III Protocol for NHS-ester dye-coupling reaction to amino allyl dUTP . Cy3 and Cy5 were purchased from GE Healthcare
 
 
Hybridization protocol Hybridizations were incubated at 65˚C for 17 hours. After hybridization slides were washed using Agilent's Wash Buffer 1 and 2.
Scan protocol Agilent Technologies DNA Microarray Scanner with Surescan High-Resolution Technology
Description Competence medium Replicate 2: A wild-type PY79 culture was grown in Competence Medium and samples were collected at 1.5 (OD600nm 0.4), 1 (OD600nm 0.4), and 0.5 (OD600nm 0.6) hours before the onset of stationary phase, the onset of stationary phase (OD600nm 0.9), and 0.5 (OD600nm 0.9), 1.5 (OD600nm 1.0), 2.5 (OD600nm 0.9), and 3.5 (O.D.600nm 1.0) hours after the onset of stationary phase. A common reference was made by pooling RNA from each time point.
Data processing Microarray data processing was performed in R (www.r-project.org) using the Bioconductor bioinformatics software package (www.bioconductor.org). Data were loaded into R using the marray package and normalized between arrays using loess normalization. Normalized log-ratios of gMedianSignal and rMedianSignal were collapsed for redundant probes taking the average.
 
Submission date Mar 18, 2015
Last update date Oct 09, 2015
Contact name Patrick Eichenberger
E-mail(s) [email protected], [email protected]
Organization name New York University
Department Center for Genomics and Systems Biology
Lab Eichenberger
Street address 12 Waverly Place
City New York
State/province New York
ZIP/Postal code 10003
Country USA
 
Platform ID GPL15179
Series (1)
GSE67023 An experimentally supported model of the Bacillus subtilis global transcriptional regulatory network.

Data table header descriptions
ID_REF
VALUE normalized log2 ratio gMedianSignal/rMedianSignal

Data table
ID_REF VALUE
BSU00010 0.205644607
BSU00020 0.303659643
BSU00030 -0.006046677
BSU00040 -0.235094024
BSU00050 -0.185188781
BSU00060 -0.053909923
BSU00070 0.101396281
BSU00080 0.219059435
BSU00090 -0.773552919
BSU00100 -0.337446058
BSU00110 -0.836730216
BSU00120 -0.653205986
BSU00130 -0.675515252
BSU00140 0.116832663
BSU00150 -0.352175671
BSU00160 -0.334977751
BSU00170 -0.896375076
BSU00180 -0.059057364
BSU00190 -0.17565068
BSU00200 -0.246311928

Total number of rows: 4657

Table truncated, full table size 98 Kbytes.




Supplementary file Size Download File type/resource
GSM1636253_US93503718_252962910022_S01_GE2_107_Sep09_1_4.txt.gz 1.5 Mb (ftp)(http) TXT
Processed data included within Sample table

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