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Items: 3

1.

Genomic Aberrations in Paediatric Gliomas and Embryonal Tumours

(Submitter supplied) The pathogenesis of paediatric central nervous system tumours is still poorly understood. In an attempt to increase the knowledge of the genetic mechanisms underlying these tumours, we performed genome-wide screening of 17 paediatric gliomas and embryonal tumours using a combination of G-band karyotyping and array comparative genomic hybridisation (aCGH). G-banding revealed abnormal karyotypes in 56% of tumour samples (9 of 16; one failed in culture), whereas aCGH analysis found copy number aberrations in all 13 tumours that could be examined. more...
Organism:
Homo sapiens
Type:
Genome variation profiling by genome tiling array
Platform:
GPL10123
13 Samples
Download data: TXT
Series
Accession:
GSE27671
ID:
200027671
2.

Agilent-022060 SurePrint G3 Human CGH Microarray 4x180K (Feature Number version)

(Submitter supplied) SurePrint G3 Human CGH Microarray 4x180K Arrays of this design have barcodes that begin with 16022060 or 2522060. Data table annotations based on build hg18:NCBI36:Mar2006. Orientation: Features are numbered numbered Left-to-Right, Top-to-Bottom as scanned by an Agilent scanner (barcode on the left, DNA on the back surface, scanned through the glass), matching the FeatureNum output from Agilent's Feature Extraction software. more...
Organism:
Homo sapiens
88 Series
1 Related Platform
1333 Samples
Download data
Platform
Accession:
GPL10123
ID:
100010123
3.

CNS-PNET 08-1118

Organism:
Homo sapiens
Source name:
Human brain (channel 1) Control_DNA_Promega (channel 2)
Platform:
GPL10123
Series:
GSE27671
Download data: TXT
Sample
Accession:
GSM685396
ID:
300685396
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