NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM1303100 Query DataSets for GSM1303100
Status Public on Aug 07, 2014
Title BF638R DM-glucose media rep3
Sample type RNA
 
Source name grown in vitro to mid-log phase in defined media with glucose
Organism Bacteroides fragilis 638R
Characteristics treatment: grown in vitro to mid-log phase in defined media with glucose
sample type: grown in vitro to mid-log phase in defined media with glucose
Growth protocol For in vitro samples: Overnight cultures of Bacteroides fragilis 638R were diluted into defined media contain either 0.5% glucose or 2% mucin glycans, and grown to mid-logarithmic phase at A550 of 0.5 complex media ( Rocha et al. 1996, J. Bacteriol. 178:6895). For in vivo samples, BF638R cells were grown in a tissue cage in rats and sampled on days 1,4, and 8 post-inoculation as described by Lobo et al. 2013, MicrobiologyOpen 2:326.
Extracted molecule total RNA
Extraction protocol Total RNA was isolated by the hot phenol method and treated as described by Sund et al, 2008, Mol. Microbiol.67:129-142.
Label Cy3
Label protocol Labeling was performed by at the FSU NimbleGen Microarray Facility, using standard protocols as described previously (Sund et al., 2008, Mol. Microbiol. 67:129-142).
 
Hybridization protocol Hybridization was performed by at the FSU NimbleGen Microarray Facility, using standard protocols as described previously (Sund et al., 2008, Mol. Microbiol. 67:129-142)
Scan protocol Scanning was performed by at the FSU NimbleGen Microarray Facility, using standard protocols as described previously (Sund et al., 2008, Mol. Microbiol. 67:129-142)
Data processing Raw data (pair files) were subjected to RMA (Robust Multi-Array Analysis; Irizarry et al. Biostatistics 4(2):249), quantile normalization (Bolstad et al. Bioinformatics 19(2):185) using NimbleGen Systems DEVA 1.1 software as described on their web site. Raw data (pair files) were subjected to RMA (Robust Multi-Array Analysis; Irizarry et al. Biostatistics 4(2):249), quantile normalization (Bolstad et al. Bioinformatics 19(2):185) using DEVA 1.1 software downloaded from Roche/NimbleGen as described on their web site (http://www.nimblegen.com/downloads/support/06271090001_DEVA_UserGuide_v1p2.pdf).
 
Submission date Jan 07, 2014
Last update date Aug 07, 2014
Contact name Charles Jeffrey Smith
E-mail(s) [email protected]
Phone 252-744-2700
Fax 252-744-3104
Organization name East Carolina University
Department Microbiology & Immunology
Street address 600 Moye Blvd.
City Greenville
State/province NC
ZIP/Postal code 27834
Country USA
 
Platform ID GPL15788
Series (1)
GSE53883 Bacteroides fragilis in vivo gene expression

Data table header descriptions
ID_REF
VALUE The RMA processed data was averaged and log2 transformed (see *.calls files)

Data table
ID_REF VALUE
BF638000000000001 10.57708
BF638000000000002 5.31924
BF638000000000003 4.34124
BF638000000000004 5.45544
BF638000000000005 7.27865
BF638000000000006 8.8874
BF638000000000007 6.94306
BF638000000000008 4.77744
BF638000000000009 5.35209
BF638000000000010 5.32979
BF638000000000011 4.60847
BF638000000000012 9.67519
BF638000000000013 5.64165
BF638000000000014 10.66829
BF638000000000015 10.54799
BF638000000000016 9.9426
BF638000000000017 10.85385
BF638000000000018 12.67052
BF638000000000019 11.71609
BF638000000000020 11.547

Total number of rows: 4341

Table truncated, full table size 111 Kbytes.




Supplementary file Size Download File type/resource
GSM1303100_DM-glucose_rep3.calls.gz 277.9 Kb (ftp)(http) CALLS
GSM1303100_DM-glucose_rep3.pair.gz 5.7 Mb (ftp)(http) PAIR
Processed data included within Sample table
Processed data provided as supplementary file

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