NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM1636119 Query DataSets for GSM1636119
Status Public on Mar 20, 2015
Title Germ1_T90min
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 1.192518767
BSU00020 1.847735866
BSU00030 1.256746448
BSU00040 1.198211134
BSU00050 0.983670304
BSU00060 1.357158448
BSU00070 1.095491523
BSU00080 0.508814727
BSU00090 -0.45342269
BSU00100 1.995801325
BSU00110 1.083401105
BSU00120 0.984200095
BSU00130 -0.331571654
BSU00140 0.21886043
BSU00150 0.482397291
BSU00160 -1.27099305
BSU00170 -1.32680025
BSU00180 -0.376109875
BSU00190 0.371000929
BSU00200 -0.318628601

Total number of rows: 4657

Table truncated, full table size 98 Kbytes.




Supplementary file Size Download File type/resource
GSM1636119_US93503718_252962910008_S01_GE2_107_Sep09_1_3.txt.gz 1.4 Mb (ftp)(http) TXT
Processed data included within Sample table

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