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Sample GSM1322536 Query DataSets for GSM1322536
Status Public on Feb 05, 2014
Title P41S2L8H3: AggressiveLocalizedAffected
Sample type RNA
Source name periodontal tissue
Organism Homo sapiens
Characteristics patient: 41
specimen: 2
biopsyid: 41.2
diagnosis: Aggressive
extent: Localized
condition: Affected
labelbatch: 8
hybridizebatch: 3
Treatment protocol Gingival tissue samples comprising pocket/sulcus epithelium and the underlying connective tissue were obtained from patients with chronic or aggressive periodontitis in conjunction with periodontal surgery
Growth protocol N/A
Extracted molecule total RNA
Extraction protocol Tissue samples were stored in liquid RNA stabilization reagent (RNAlater, Austin, TX) overnight at 4°C, snap-frozen and stored in liquid nitrogen. Specimens were homogenized in Trizol (Invitrogen Life Technologies, Carlsbad, CA), incubated with chloroform and centrifuged at 12,000g. RNA collected in the upper aqueous phase was precipitated by mixing with 75% isopropyl-alcohol and additional centrifugation and washings, and was quantified spectrophotometrically. RNA quality was assessed by determining the RNA Integrity Number (RIN).
Label cyanine 3-pCp
Label protocol miRNA profiling was carried out using the Agilent platform (Agilent Technologies). Total RNA (100 ng/specimen) was labeled to generate fluorescent miRNA by ligation of cyanine 3-pCp to the 3’end
Hybridization protocol Labeled RNA hybridized with microarrays carrying probes for 1,205 human and 144 human viral miRNAs (SurePrint G3 Human v16 miRNA 8x60K Microarray Kit).
Scan protocol Array images were scanned with Agilent Technologies Scanner G2505C US83000178 using grid 031181_D_F_20110707 and protocol miRNA_105_Dec08.
Description P41S2L8H3
Data processing The scanned images were analyzed with Feature Extraction Software (Agilent) using 031181_D_F_20110707.xml as design file to obtain background subtracted and Processed Signal intensities. Subsequent data analysis and normalization was performed within R/Bioconductor. Data was normalized and background corrected using rmaMicroRna function with background and normalize set to TRUE. Filtering was performed according to the recommended AgiMicroRna documentation having the following filterMicroRna parameters:
control = TRUE,
IsGeneDetected = TRUE,
wellaboveNEG = FALSE,
limIsGeneDetected = 75,
limNEG = 25
Submission date Feb 05, 2014
Last update date Feb 06, 2014
Contact name Paolo Guarnieri
Organization name Columbia University
Department Systems Biology
Street address 1130 St. Nicholas Avenue
City New York
State/province NY
ZIP/Postal code 10032
Country USA
Platform ID GPL15159
Series (1)
GSE54710 MicroRNAs and their target genes in gingival tissues.

Data table header descriptions
VALUE RMA Normalized signal intensity as computed with AgiMicroRna bioconductor package.

Data table
A_25_P00015345 2.356354032
A_25_P00015343 2.308683076
Blank 1.934398564
dmr_285 10.42738058
dmr_3 14.17954533
dmr_308 2.445143012
dmr_316 2.810806787
dmr_31a 10.26019239
dmr_6 12.57947124
A_25_P00013722 2.530443806
A_25_P00013718 2.347851304
A_25_P00011668 2.459082904
A_25_P00013809 2.669881085
A_25_P00011834 2.339830539
A_25_P00013749 2.372617103
A_25_P00013752 4.93805984
A_25_P00011853 4.60427311
A_25_P00013814 2.328404184
A_25_P00014783 2.339840459
A_25_P00011886 2.380929018

Total number of rows: 1368

Table truncated, full table size 35 Kbytes.

Supplementary file Size Download File type/resource
GSM1322536_US83000178_253118110685_S01_miRNA_105_Dec08_2_3.txt.gz 8.0 Mb (ftp)(http) TXT
Processed data included within Sample table

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