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Sample GSM2107655 Query DataSets for GSM2107655
Status Public on Sep 26, 2016
Title ETV6-RUNX1-10
Sample type RNA
 
Source name bone marrow
Organism Homo sapiens
Characteristics diagnosis: b-cell precursor acute lymphoblastic leukemia (BCP-ALL)
Extracted molecule total RNA
Extraction protocol Total RNA was harvested with the miRNeasy mini kit (Qiagen) with Dnase treatment on-column.
Label Cy3
Label protocol Cyanine-3 (Cy3) labeled cRNA was prepared from 100 ng RNA using the One-Color Low Input Quick Amp Labling kit (Agilent) according to the manufacturer's instructions, followed by miRNeasy column purification (Qiagen). Dye incorporation and cRNA yield were checked with the NanoDrop ND-1000 Spectrophotometer.
 
Hybridization protocol 600 ng of Cy3-labelled cRNA (specific activity >6 pmol Cy3/ug cRNA) was fragmented at 60°C for 30 minutes in a reaction volume of 25µl containing 1x Agilent fragmentation buffer and 2x Agilent blocking agent following the manufacturers instructions. On completion of the fragmentation reaction, 25 µl of 2x GEx Hybridization buffer HI-RPM was added to the fragmentation mixture and hybridized to the array for 17 hours at 65°C in a rotating hybridization oven. After hybridization, microarrays were washed 1 minute at room temperature with GE Wash Buffer 1 (Agilent) and 1 minute with 37°C GE Wash buffer 2 (Agilent).
Scan protocol Slides were scanned immediately after washing on the Agilent DNA Microarray Scanner with SureScan High-Resolution Technology using one color scan setting for 8x60k array slides (Scan Area 61x21.6 mm, Scan resolution 3µm, Dye channel is set to Green).
Description Gene expression of T-ALL patient bone marrow sample
Data processing The scanned images were analyzed with Feature Extraction Software (Agilent) using default parameters (protocol GE1-105_Dec08 and Grid: 041648_D_F_20120615) to obtain background subtracted and spatially detrended Processed Signal intensities.
 
Submission date Apr 04, 2016
Last update date Sep 26, 2016
Contact name Farzaneh Ghazavi
E-mail(s) farzaneh.ghazavi@ugent.be
Organization name Gent university hospital
Department Center of medical genetics
Street address De Pintelaan 185
City Ghent
ZIP/Postal code 9000
Country Belgium
 
Platform ID GPL19197
Series (2)
GSE79869 Lnc-RNA expression pattern in ETV6/RUNX1-driven b-cell precursor acute lymphoblastic leukemia (BCP-ALL)
GSE79873 Unique long non-coding RNA expression signature in ETV6/RUNX1-driven B-cell precursor acute lymphoblastic leukemia

Data table header descriptions
ID_REF
VALUE Normalized signal intensity.

Data table
ID_REF VALUE
A_33_P3400429 6.752299233
A_33_P3255531 4.201805672
A_24_P940149 5.615467857
A_33_P3306510 10.48623669
CUST_21085_PI427704219 2.719237288
A_33_P3348313 9.419064247
A_33_P3403361 9.948585179
A_33_P3348973 8.073831177
A_23_P11070 7.168816853
A_24_P274615 9.573620927
CUST_1480_PI427704219 3.979673288
CUST_13414_PI427704219 4.778711966
A_24_P928969 1.170357203
A_23_P100074 9.142207665
A_33_P3227506 7.619034357
CUST_17237_PI427704219 8.453870463
CUST_12234_PI427704219 3.002281351
A_32_P47643 2.557429187
CUST_802_PI427704219 3.590609751
A_33_P3542886 4.342177321

Total number of rows: 43357

Table truncated, full table size 1191 Kbytes.




Supplementary file Size Download File type/resource
GSM2107655_ETV6-RUNX1-10.txt.gz 3.1 Mb (ftp)(http) TXT
Processed data included within Sample table

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