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Sample GSM1093551 Query DataSets for GSM1093551
Status Public on Jun 21, 2014
Title BRCAX_06T238
Sample type RNA
 
Source name hereditary invasive breast cancer
Organism Homo sapiens
Characteristics storage: formalin-fixed parafin-embeded tissue
tumor type: BRCAX 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) tanic.miljana@gmail.com
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 8.83986044
17888 6.745390344
42769 6.86271414
17749 9.320478342
19004 10.04712788
46437 8.023029178
46436 9.77172369
46435 9.841010248
46438 7.716376167
9938 7.733441345
19581 6.464178161
31026 6.943604396
10919 7.324363387
42648 6.622607678
19582 7.00624821
10923 7.113002561
13485 6.660016389
46258 7.177666868
46345 6.94280636
19583 7.517340145

Total number of rows: 444

Table truncated, full table size 7 Kbytes.




Supplementary file Size Download File type/resource
GSM1093551_US22502553_14125143_S01_fliped_Exiqon_SingleColor.txt.gz 796.1 Kb (ftp)(http) TXT
Processed data included within Sample table

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