NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM2486545 Query DataSets for GSM2486545
Status Public on Sep 14, 2017
Title sample.10.SP_post-S
Sample type RNA
 
Source name post-S
Organism Homo sapiens
Characteristics subject status: patients with Barrett's oesophagus who underwent APC ablation of their Barrett's mucosa
tissue: post-ablation Proximal squamous mucosa
percentage of barrett's at 3-5 years: N/A
molecule subtype: microRNA
Treatment protocol Musocal biopsy samples were collected from patients with Barrett's oesophagus or healthy controls. After collection, they were immediately stored in RNAlater® solution (Ambion, Austin, Texas, USA) as the manufacturer’s protocol indicated
Extracted molecule total RNA
Extraction protocol After the biopsies were thawed and extra RNAlater@ solution removed, the samples were homogenized in 500 ul TRIzol@ Reagent (Invitrogen, Carlsbad, CA, USA) and the manufacturer's protocol was followed to extract RNA. The RNA concentration was determined using the Biophotometer.
Label FAMTM
Label protocol PCR assays were performed by following the protocol for TaqMan@OpenArray Human MicroRNA Panel (4461104, Life technologies). 45 ng of RNA was used in the reverse transciption reaction for each sample. Megaplex Primer pools, Human Pools set v3.0 was used in the assay.
 
Hybridization protocol n/a
Scan protocol n/a
Data processing Raw fluorescence data was processed using OpenArray® Real-Time qPCR Analysis Software (BioTrove™, version 1.0.4). Raw fluorescence data was exported in .csv file format for subsequent processing in R software.
The CSV files were imported into R software (3.1.0) and the fractional cycle (Ct) at which the second derivative maximum of a logistic curve fit to the raw fluorescence data was determined. Any microRNA that had no Ct value for a particular sample was assigned the value of 40.
Mann Whitney U tests were used to generate lists of differentially expressed microRNAs in the comparison of control squamous tissues vs post-ablation neosquamous tissues, and for the comparison of post-ablation squamous tissues vs. post-ablation neosquamous tissues. Significance was set at p<0.05.
False Discovery rates were estimated using the Benjamini-Hochberg procedure (Benjamini, Yoav; Hochberg, Yosef (1995). Controlling the false discovery rate: a practical and powerful approach to multiple testing (PDF). Journal of the Royal Statistical Society, Series B. 57 (1): 289–300.)
Fold Change worksheet reports the the ratios of normalized relative expression levels.
 
Submission date Feb 14, 2017
Last update date Sep 14, 2017
Contact name Damian James Hussey
E-mail(s) damian.hussey@flinders.edu.au
Organization name Flinders University
Street address Flinders Drive
City Bedford Park
ZIP/Postal code 5042
Country Australia
 
Platform ID GPL17485
Series (1)
GSE94854 The microRNA profile in neosquamous oesophageal mucosa following ablation of Barrett's oesophagus

Data table header descriptions
ID_REF
VALUE normalized relative levels

Data table
ID_REF VALUE
000604_hsa-miR-424 0.000705081
002332_hsa-miR-409-3p 0.157031528
002261_hsa-miR-135b 1.155484116
002279_hsa-miR-31 1.655680135
000460_hsa-miR-135a 0.50426648
001193_mmu-miR-187 0.917482768
002098_hsa-miR-223# 0.0011178
002122_hsa-miR-376c 0.146128379
002293_hsa-miR-214# 0.158926301
000452_hsa-miR-127 0.188532382
002100_hsa-miR-136# 0.243897718
000498_hsa-miR-199a 0.000328403
002113_hsa-miR-31# 2.324329301
000545_hsa-miR-331 0.85100005
001551_hsa-miR-597 0.745806682
002309_hsa-miR-424# 1.366345048
001610_hsa-miR-411 0.178166918
000426_hsa-miR-34a 0.770428512
000456_hsa-miR-130b 0.746288927
002215_hsa-miR-196b 0.172829638

Total number of rows: 750

Table truncated, full table size 23 Kbytes.




Supplementary data files not provided
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