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Sample GSM412757 Query DataSets for GSM412757
Status Public on Jun 27, 2009
Title 1558_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 9.645850482
hsa-let-7b 12.09055585
hsa-let-7b* 2.041029066
hsa-let-7c 9.911115032
hsa-let-7d 7.134971629
hsa-let-7d* 4.373118497
hsa-let-7e 9.209378977
hsa-let-7f 8.171097217
hsa-let-7f-1*
hsa-let-7g 6.19676554
hsa-let-7i 6.773945207
hsa-miR-100 2.273865082
hsa-miR-101 2.463212979
hsa-miR-103 6.969883089
hsa-miR-105 1.834964486
hsa-miR-106a
hsa-miR-106b 4.610388616
hsa-miR-106b* 2.237049923
hsa-miR-107 7.192234958
hsa-miR-10a 2.129622875

Total number of rows: 319

Table truncated, full table size 7 Kbytes.




Supplementary file Size Download File type/resource
GSM412757.txt.gz 1.8 Mb (ftp)(http) TXT
Processed data included within Sample table

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