NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM2450917 Query DataSets for GSM2450917
Status Public on Apr 18, 2017
Title sputum from lung cancer patient 4 (dye flip)
Sample type RNA
 
Channel 1
Source name sputum from lung cancer patient 4
Organism uncultured bacterium
Characteristics bacterial strain: speciation not done
human tissue source: sputum
diagnosis: lung cancer
Treatment protocol Expectorated sputum were immediately transferred to Primestore molecular transport media after collection.
Growth protocol For using as reference, M. tb H37Rv was grown in Middlebrook 7H9 broth to mid-log phase
Extracted molecule total RNA
Extraction protocol Sputum samples after collection were immediately transferred to Primestore molecular transport media (Longhorn vaccines and diagnostics). Total RNA from sputum samples in primestore was isolated using RNAzol as per manufacturer's protocol. An RNA amplification strategy was used (MessageAmp II-bacteria RNA amplification kit- Ambion) (Schlingemann etal., 2005; Garton et al., 2008)
Label Cy3
Label protocol The synthesis and fluorescent labeling of cDNA with Cy3 or Cy5 from aRNA was accomplished by first performing reverse transcriptase (RT) reaction with Superscript II RT followed by labeling with Klenow fragment using Bioprime Kit (Invitrogen) following a published method (Schlingemann 2005).
 
Channel 2
Source name 7H9 broth-grown M. tb
Organism Mycobacterium tuberculosis
Characteristics bacterial strain: H37Rv
human tissue source: none (broth-grown)
Treatment protocol Expectorated sputum were immediately transferred to Primestore molecular transport media after collection.
Growth protocol For using as reference, M. tb H37Rv was grown in Middlebrook 7H9 broth to mid-log phase
Extracted molecule total RNA
Extraction protocol Sputum samples after collection were immediately transferred to Primestore molecular transport media (Longhorn vaccines and diagnostics). Total RNA from sputum samples in primestore was isolated using RNAzol as per manufacturer's protocol. An RNA amplification strategy was used (MessageAmp II-bacteria RNA amplification kit- Ambion) (Schlingemann etal., 2005; Garton et al., 2008)
Label Cy5
Label protocol The synthesis and fluorescent labeling of cDNA with Cy3 or Cy5 from aRNA was accomplished by first performing reverse transcriptase (RT) reaction with Superscript II RT followed by labeling with Klenow fragment using Bioprime Kit (Invitrogen) following a published method (Schlingemann 2005).
 
 
Hybridization protocol For hybridization, labeled cDNA probes generated from aRNA obtained from M. tb in PTB patient sputum was mixed with the labeled reference cDNA probe prior to purification with Microcon YM10 filter (Millipore). For each sputum sample from PTB patients, the M. tb arrays were hybridized over night with the mixed labeled cDNA probes including a Cy3/Cy5 dye swap for 4/7 samples (Fontan et al, 2008)
Scan protocol The microarrays were scanned and processed with an Axon 4000B scanner and GenePix Pro 6.1 software, respectively.
Data processing Normalized by the print-tip Lowess method; intensity ratio data obtained used to perform Significance Analysis of Microarrays (SAM) with Multiarray Viewer Software on the TMEV website for determination of differentially expressed genes; ≥ 2 fold change at a false discovery rate of < 2% were considered significantly differentially expressed.
 
Submission date Jan 09, 2017
Last update date Apr 18, 2017
Contact name Indu Verma
E-mail(s) [email protected]
Phone 09815177700
Organization name Post Graduate Institute of Medical Education and Research (PGIMER)
Department Biochemistry
Lab 310
Street address Dept. of Biochemistry, PGIMER
City Chandigarh
State/province Outside U.S. & Canada
ZIP/Postal code 160012
Country India
 
Platform ID GPL4057
Series (1)
GSE93316 Transcriptome analysis of mycobacteria in sputum samples of pulmonary tuberculosis patients

Data table header descriptions
ID_REF
VALUE normalized ratio representing test/reference

Data table
ID_REF VALUE
010101 0.878441
010102 0.710216
010103 -0.296117
010104 0.187712
010105 0.264934
010106 0.518175
010107 0.764778
010108 0.366793
010109 0.468051
010110 0.37322
010111 0.4224
010112 0.470186
010113 0.616937
010114 0.472052
010115 0.486511
010201 0.746582
010202 0.473727
010203 0.532114
010204 -1.90738
010205 -0.506404

Total number of rows: 4296

Table truncated, full table size 69 Kbytes.




Supplementary file Size Download File type/resource
GSM2450917_SLC3_Rv5-norm_-.gpr.gz 580.2 Kb (ftp)(http) GPR
Processed data included within Sample table
Processed data are available on Series record

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