NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM1636118 Query DataSets for GSM1636118
Status Public on Mar 20, 2015
Title Germ1_T70min
Sample type RNA
 
Channel 1
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 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 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 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 Germination in DSM Replicate 1: A wild-type PY79 culture was grown in Difco Sporulation Medium (DSM) for 72 hours and spores were harvested. The purified spores were germinated in DSM and samples were collected at 40, 70, 90, 120, and 150 minutes. 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) pe19@nyu.edu, arb401@nyu.edu
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 -0.413118634
BSU00020 -0.490629168
BSU00030 -0.725699887
BSU00040 -0.24729133
BSU00050 -0.583630567
BSU00060 -0.311989711
BSU00070 -0.132120746
BSU00080 0.194049067
BSU00090 -0.094240928
BSU00100 0.228820493
BSU00110 0.72127419
BSU00120 0.404434534
BSU00130 0.167698731
BSU00140 -0.467464606
BSU00150 -0.429473209
BSU00160 3.093744118
BSU00170 3.896461416
BSU00180 -0.52949525
BSU00190 0.008752992
BSU00200 0.077804865

Total number of rows: 4657

Table truncated, full table size 98 Kbytes.




Supplementary file Size Download File type/resource
GSM1636118_US93503718_252962910008_S01_GE2_107_Sep09_1_4.txt.gz 1.5 Mb (ftp)(http) TXT
Processed data included within Sample table

| NLM | NIH | GEO Help | Disclaimer | Accessibility |
NCBI Home NCBI Search NCBI SiteMap