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Sample GSM2107700 Query DataSets for GSM2107700
Status Public on Sep 26, 2016
Title Normal karyo-8
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 blood 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 6.807271597
A_33_P3255531 5.056447102
A_24_P940149 5.255052591
A_33_P3306510 11.08039088
CUST_21085_PI427704219 3.093679714
A_33_P3348313 9.455435266
A_33_P3403361 9.931588185
A_33_P3348973 7.683274494
A_23_P11070 4.761002924
A_24_P274615 7.072082281
CUST_1480_PI427704219 4.013347661
CUST_13414_PI427704219 4.501748387
A_24_P928969 3.158629979
A_23_P100074 8.773758028
A_33_P3227506 7.750791017
CUST_17237_PI427704219 8.937561354
CUST_12234_PI427704219 2.88123471
A_32_P47643 2.135025813
CUST_802_PI427704219 2.637023303
A_33_P3542886 4.60207329

Total number of rows: 43357

Table truncated, full table size 1190 Kbytes.




Supplementary file Size Download File type/resource
GSM2107700_Normal_karyo-8.txt.gz 3.0 Mb (ftp)(http) TXT
Processed data included within Sample table

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