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Sample GSM1093535 Query DataSets for GSM1093535
Status Public on Jun 21, 2014
Title BRCA1_02T124
Sample type RNA
 
Source name hereditary invasive breast cancer
Organism Homo sapiens
Characteristics storage: formalin-fixed parafin-embeded tissue
tumor type: BRCA1 breast tumor
Extracted molecule total RNA
Extraction protocol For each sample tumoral area was marked by pathologist, FFPE blocks were cut in 5x 30µm sections and tumor tissue was isolated by needle macrodissection for subsequent RNA extraction. Total RNA was extracted using miRNeasy FFPE kit (QIAGEN) according to manufacturer’s instructions, while tissue digestion step was performed using 20 mg/ul Proteinase K (Roche, Basel, Switzerland) for over-night incubation step at 55ºC. RNA quantity was assessed by NanoDrop Spectrophotometer (Nanodrop Technologies, Wilmington, DE, USA).
Label Hy3
Label protocol 300ng of total RNA were treated for with Calf Intestine Phosphatase and than labeled with Hy3 fluorescent dye according to manufacturers instructions.
 
Hybridization protocol Denaturated Hy3 labeled RNA samples in 1x hybridization buffer were hybridized at 56ºC for 16h onto Exiqon miRNA microarray slides (v.11.0 – hsa, mmu & rno) containing 1940 capture probes in 4 replicates, including 830 human miRNAs annotated in miRBasev.11 database and 434 hsa- miRPlus probes. A set of 10 synthetic spike-in RNAs was added to total RNA sample prior to labeling and later used for quality control.
Scan protocol Processed slides were scanned with Agilent Array scanner (Agilent Technologies, Santa Clara, CA, USA), with the laser set to 635nm, at Power 80 and PMT 70 setting, and a scan resolution of 10μm.
Data processing Fluorescence intensities on scanned images were quantified using Feature Extraction software (Agilent Technologies, Santa Clara, CA, USA) using the modified Exiqon protocol. Average processed intensity values of the replicate spots were background subtracted using Normexp, and log2 transformed. Raw data were quantile normalized for inter-array variability using R/Bioconductor. Data was further processed to eliminate miRNAs with uniformly low expression (<6.5) or with low expression variation (VAR<0.1) across the experiments, retaining 444 miRNA genes (276 hsa-miR + 168 hsa-miRPlus).
 
Submission date Mar 05, 2013
Last update date Jun 21, 2014
Contact name Miljana Tanic
E-mail(s) [email protected]
Organization name Institute for Oncology and Radiology of Serbia (IORS)
Department Experimental Oncology
Lab Laboratory of Molecular Genetics
Street address Pasterova 14
City Belgrade
ZIP/Postal code 11000
Country Serbia
 
Platform ID GPL7723
Series (1)
GSE44899 miRNA expression profiling in hereditary breast tumors

Data table header descriptions
ID_REF
VALUE Quantile-normalized log2 transformed signal intensity

Data table
ID_REF VALUE
17748 8.416848748
17888 6.430680237
42769 6.711875132
17749 8.483889211
19004 9.744591486
46437 7.877615103
46436 9.459228116
46435 9.329106107
46438 7.53283592
9938 7.403120628
19581 6.709788328
31026 7.243888811
10919 7.665009456
42648 6.666690216
19582 6.882544515
10923 7.36233499
13485 7.554946956
46258 7.070393918
46345 6.685740628
19583 6.802564704

Total number of rows: 444

Table truncated, full table size 7 Kbytes.




Supplementary file Size Download File type/resource
GSM1093535_US22502553_14110847_S01_fliped_Exiqon_SingleColor.txt.gz 796.8 Kb (ftp)(http) TXT
Processed data included within Sample table

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