E-MTAB-2340 - Comparative genomic hybridization by array of human high grade glioma sample and control DNA using a custom oligonucleotide array
Released on 1 March 2014, last updated on 13 May 2014
Custom oligonucleotide array CGH. We designed two fine-tiling oligonucleotide microarrays to cover the specific amplicons observed at chromosome 2p22.1 and 10q11.21 This was undertaken using the Agilent custom array design tool e-Array (Agilent, Santa Clara, CA, USA; https://earray.chem.agilent.com/), and comprised 700 probes covering 43.56Ð43.70 Mb on chromosome 10 and 5000 probes covering 39Ð40 Mb on chromosome 10 with a median probe interval of 200 bp on 2x105K microarray. Due to limited amount of material, DNA was whole genome amplified (WGA) using the GenomePlex Complete Whole Genome Amplification Kit (Sigma, Gillingham, UK) starting with 10 ng of sample and control DNA, and following the manufacturers protocol. WGA DNA was labelled using the Agilent Genomic DNA ULS labelling kit, hybridised as per manufacturers instructions, and scanned on the Agilent 2505B Microarray Scanner System.
comparative genomic hybridization by array, disease state design
The prognostic role of intragenic copy number breakpoints and identification of novel fusion genes in paediatric high grade glioma. Carvalho D, Mackay A, Bjerke L, Grundy RG, Lopes C, Reis RM, Jones C. :23 (2014), Europe PMC 24548782
The prognostic role of intragenic copy number breakpoints and identification of novel fusion genes in paediatric high grade glioma. Diana Carvalho, Alan Mackay, Lynn Bjerke, Richard G Grundy, Celeste Lopes, Rui M Reis and Chris Jones.