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Sample GSM1713778 Query DataSets for GSM1713778
Status Public on Jun 18, 2015
Title breast cancer_control [Patient 2]
Sample type RNA
 
Source name patients without local relapse after breast conserving therapy in early stage breast cancer
Organism Homo sapiens
Characteristics patient id: Patient 2
gender: female
tissue type: primary tumor
sample type: FFPE material
Treatment protocol breast cancer tissue from surgical procedure
Extracted molecule total RNA
Extraction protocol slices from FFPE samples were sent to the comprehensive biomarker center (cbc™) in Heidelberg, RNA was extracted according to cbc standard procedures
Label Cy3
Label protocol 100 ng total RNA input per array, for labeling Agilent's microRNA Complete labeling and Hybridization Kit was used; the protocol followed cbc™ standard procedures
 
Hybridization protocol hybridization time was 20h at 55° with 20rpm following cbc™ standard procedures
Scan protocol Scanning and image acquisition followed cbc™ standard procedures; Scanner: Latest High-Resolution Microarray Scanner GS2505_C
Data processing The scanned images were analyzed with the latest Agilent Feature Extraction software (10.7.3.1) according to cbc™ standard procedures. To detect outliers in the samples, Hampel's rule was applied. For this purpose all correlation coefficients were transformed using the Fisher transformation and then applied the robust test for detecting outliers. The RMA (robust multi-arra average) was used for normalization.
The RMA algorithm calculates an own background, normalizes by quantile and summarizes the data. The first step is a background correction by fitting a normal and exponential convolution model to the vector of observed intensities. The normal part represents the background, the exponential part represents the signal intensities. After background subtraction the arrays are normalized by quantile across a set of hybridizations at the probe level. Finally an estimate of the microRNA gene signal is obtained by fitting a linear model to log 2 transformed intensities. This procedure was carried out by cbcT.
 
Submission date Jun 17, 2015
Last update date Jun 18, 2015
Contact name Franz Zehentmayr
E-mail(s) f.zehentmayr@salk.at
Organization name RadArt
Street address Müllner Hauptstraße
City Salzburg
ZIP/Postal code 5020
Country Austria
 
Platform ID GPL16770
Series (1)
GSE69951 Hsa-miR-375 in early breast cancer

Data table header descriptions
ID_REF
VALUE normalize signal intensity according to RMA

Data table
ID_REF VALUE
ebv-miR-BART12 8.18603965456342
ebv-miR-BART13 570.451711285315
ebv-miR-BART16 12.5805973956589
ebv-miR-BART19-3p 206.914878696243
ebv-miR-BART7 8.89157635946415
ebv-miR-BHRF1-1 7.82462186840325
hbv-miR-B20 26.3144053715464
hbv-miR-B2RC 21.3646703911921
hbv-miR-B4 14.6783724181401
hcmv-miR-UL70-3p 149.701923487218
hcmv-miR-US4 36.7932440205758
hiv1-miR-H1 22.7474293359824
hsa-let-7a 5936.93636281803
hsa-let-7b 5543.92528759121
hsa-let-7b* 11.0352477291216
hsa-let-7c 1316.24952884779
hsa-let-7d 355.285110550958
hsa-let-7d* 6.60630623782894
hsa-let-7e 726.143535244957
hsa-let-7f 2448.65452114101

Total number of rows: 470

Table truncated, full table size 13 Kbytes.




Supplementary file Size Download File type/resource
GSM1713778_US10523865_253118113980_S01_miRNA_1100_Jul11_2_4.txt.gz 7.9 Mb (ftp)(http) TXT
Processed data included within Sample table

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