|
Status |
Public on Mar 07, 2021 |
Title |
Control (DMSO), biological replicate 1 |
Sample type |
RNA |
|
|
Source name |
DIPG neurosphere, control without treatment
|
Organism |
Homo sapiens |
Characteristics |
treatment: control
|
Treatment protocol |
72 hours after incubation, cells were treated for 24 hours with DMSO or 1?M CBL0137.
|
Growth protocol |
HSJD-DIPG007 cells were cultured in DMEM/F12 and Neurobasal media (1:1) supplemented with HEPES, non-essential amino acids, antibiotic/antimycotic, pyruvate, glutamax, heparin, B27, human EGF, human FGF, PDGF-AA and PDGF-BB for 72 hours to form neurospheres.
|
Extracted molecule |
total RNA |
Extraction protocol |
RNA was extracted using the RNeasy extraction kit (Qiagen; Cat No./ID: 74106) according to the manufacturer’s instruction.
|
Label |
biotin
|
Label protocol |
As per Affymetrix protocol
|
|
|
Hybridization protocol |
As per Affymetrix protocol
|
Scan protocol |
As per Affymetrix protocol
|
Description |
Gene expression data from DIPG cancer cells, control without treatment
|
Data processing |
The probes from the hugene20st microarray were assigned to Ensembl Genes using custom chip definition file (CDF) hugene20sthsensgcdf (version 24.0.0) from (http://mbni.org/customcdf/24.0.0/ensg.download/hugene20sthsensgcdf_24.0.0.tar.gz). Data was analysed using Bioconductor/R, the RMA algorithm was used for array normalization, and batch effects were removed using remove unwanted variation (ruv) library and the RUVIII function with one unwanted factor (k=1).
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|
|
Submission date |
Jul 06, 2020 |
Last update date |
Mar 09, 2021 |
Contact name |
Chi Nam Ignatius Pang |
E-mail(s) |
[email protected]
|
Organization name |
The University of New South Wales
|
Department |
The NSW Systems Biology Initiative
|
Lab |
Wilkins Lab
|
Street address |
School of Biotechnology and Biomolecular Sciences, UNSW Australia
|
City |
Sydney |
State/province |
NSW |
ZIP/Postal code |
2052 |
Country |
Australia |
|
|
Platform ID |
GPL28835 |
Series (1) |
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