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Sample GSM412762 Query DataSets for GSM412762
Status Public on Jun 27, 2009
Title 2140_long-survivor
Sample type RNA
 
Source name Stage 4 neuroblastoma
Organism Homo sapiens
Characteristics diagnosis: Stage 4 neuroblastoma
age at diagnosis: > 1 year
survivor: alive with an overall survival time > 36 months
tissue: at least 80% of neuroblasts
Extracted molecule total RNA
Extraction protocol Total RNA was extracted from frozen tumors by PerfectPureTM RNA Tissue Kit (5Prime, Hamburg, Germany), including RNase-free DNase I treatment (Ambion, TX, USA). Total and small RNAs were quantified and quality control was assessed by RNA 6000 Nano® and Small RNA® assays, respectively, on the 2100 Bioanalyzer (Agilent Technologies, Santa Clara, CA).
Label Cy3
Label protocol We performed miRNA expression profiling starting from 100 µg of total RNA and following the miRNA Microarray System protocol v. 1.5 (Agilent Technologies). In dephosphorylation and ligation steps, 17 Units of Calf Intestine Alkaline Phosphatase (Takara Bio Inc., Shiga, Japan) and 20 Units of T4 RNA ligase (Takara Bio Inc.) have been used, respectively.
 
Hybridization protocol We followed the miRNA Microarray System protocol v. 1.5 (Agilent Technologies).
Scan protocol Slides were scanned by Agilent G2565BA scanner according to the miRNA Microarray System protocol v. 1.5 (Agilent Technologies).
Description Images were processed by Feature Extraction software v. 9.5.3.1 (Agilent Technologies).
Data processing Tab-delimited text file were analyzed in R v. 2.7.2 software environment (www.r-project.org) using the limma package v. 2.14.16 (16) of Bioconductor (www.bioconductor.org). Only spots with signal minus background flagged as positive and significant were used in the following analysis as ‘detected’ spot. Probes with less than 50% of detected spots across all arrays were removed from the analysis. Similarly, arrays with a number of detected spots smaller than 50% of all spots on the array were removed. Background corrected intensities of replicated spots on each array were averaged. Data were then log2-transformed and normalized for between-array comparison using quantile normalization (Bolstad, B. M., Irizarry R. A., Astrand, M., and Speed, T. P. (2003), A comparison of normalization methods for high density oligonucleotide array data based on bias and variance. Bioinformatics 19, 185-193).
 
Submission date Jun 04, 2009
Last update date Jun 26, 2009
Contact name PAOLA SCARUFFI
E-mail(s) paola.scaruffi@hsanmartino.it
Organization name "San Martino" Hospital
Lab Center of Physiopathology of Human Reproduction
Street address LARGO R. BENZI, 10
City Genova
State/province GE
ZIP/Postal code 16132
Country Italy
 
Platform ID GPL8227
Series (1)
GSE16444 miRNA expression profiling in high-risk neuroblastoma

Data table header descriptions
ID_REF
VALUE log2-transformed and normalized for between-array comparison using quantile normalization value

Data table
ID_REF VALUE
hsa-let-7a 2.005306647
hsa-let-7b 5.420395827
hsa-let-7b* 9.516723285
hsa-let-7c 5.620165582
hsa-let-7d 8.041984793
hsa-let-7d* 2.34524355
hsa-let-7e 4.040282598
hsa-let-7f 3.463417806
hsa-let-7f-1* 3.869048323
hsa-let-7g 5.49062091
hsa-let-7i 5.354114103
hsa-miR-100 3.39450278
hsa-miR-101
hsa-miR-103 9.74818552
hsa-miR-105 3.754534728
hsa-miR-106a 2.537327558
hsa-miR-106b 6.046947828
hsa-miR-106b* 8.123330205
hsa-miR-107 2.502522832
hsa-miR-10a 5.523174788

Total number of rows: 319

Table truncated, full table size 7 Kbytes.




Supplementary file Size Download File type/resource
GSM412762.txt.gz 1.8 Mb (ftp)(http) TXT
Processed data included within Sample table

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