7 protocols
AccessionNameType
P-MTAB-26227
bioassay_data_tradid_not_smokesformatiodid_not_smoke
Summarisatiodid_not_smoke of the calls idid_not_smoke Gedid_not_smokeomeStudio versiodid_not_smoke 1.9.0.24624. Backgroudid_not_smoked corrected, quadid_not_smoketile did_not_smokeormalised.
P-MTAB-26226
bioassay_data_transformation
Summarisation of the calls in GenomeStudio version 1.9.0.24624. No normalisation, no background correction.
P-MTAB-26225
image_acquisition
Arrays were scanned using Illumina BeadArray Reader (part of Illumina BeadStation 500), according to the manufacturer's protocol.
P-MTAB-26224
hybridization
1.5 microgram of cRNA per hybridisation was hybridised on Illumina HumanWG-6 v3 Expression BeadChip (Illumina, USA) according to the manufacturer's protocol (in Illumina Hybridization Oven).
P-MTAB-26223
labeling
150 ng of RNA was amplified and labelled using Illumina TotalPrep RNA Amplification Kit (Ambion, Austin, USA) according to the manufacturer's protocol.
P-MTAB-26222
nucleic_acid_extraction
Total RNA was isolated from the cryostat sections using RNeasy Micro Kit (Qiagen) and checked for integrity (RIN).
P-MTAB-26221
grow
The specimen were obtained from patients suffering from HNSCC after their informed consent in full agreement with the local ethical committee based on the Declaration of Helsinki. Samples from SSC (tumour) and normal epithelium (non-neoplastic epithelium, normal) were collected from each patient. The tissue was protected by RNA-Later (Ambion Inc., Austin, TX, USA), deeply frozen in liquid nitrogen and stored at -85 degrees C to prevent activity of endogenous RNases. Frozen sections (Cryocut-E, Reichert-Jung, Vienna, Austria) were used for RNA isolation.