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Status |
Public on Mar 23, 2012 |
Title |
SNP data from 13 childhood adrenocortical tumours from Brazilian patients and 6 matched normal samples |
Organism |
Homo sapiens |
Experiment type |
Genome variation profiling by SNP array
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Summary |
SNP array data from 13 Brazilian childhood adrenocortical tumors (ACTs) were analyzed to detect recurrent copy number changes and highlight potential candidate driver genes.
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Overall design |
13 childhood ACT were analyzed with Illumina HumanCNV370-Duo v1.0 chips. Paired normal blood samples from 6 patients were analyzed with Illumina HumanCNV370-Quad v3.0 chips.
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Contributor(s) |
Letouzé E, Rosati R, Doghman M, Mas J, Zambetti GP, Figueiredo BC, Lalli E |
Citation(s) |
22567117, 22539591 |
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Submission date |
Oct 19, 2010 |
Last update date |
Jan 30, 2015 |
Contact name |
Eric Letouzé |
E-mail(s) |
Eric.letouze@inserm.fr
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Organization name |
Ligue Contre Le Cancer
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Lab |
Centre de Recherche des Cordeliers
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Street address |
15 rue de l'école de médecine
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City |
Paris |
ZIP/Postal code |
75006 |
Country |
France |
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Platforms (2) |
GPL6985 |
Illumina HumanCNV370-QuadV3 DNA Analysis BeadChip (HumanCNV370-QuadV3_C) |
GPL6986 |
Illumina HumanCNV370-Duov1 DNA Analysis BeadChip (HumanCNV370v1) |
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Samples (19)
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This SubSeries is part of SuperSeries: |
GSE32206 |
Identity by descent mapping of founder mutations in cancer using high-resolution tumor SNP data |
GSE35066 |
SNP array profiling of childhood adrenocortical tumours reveals distinct pathways of tumourigenesis and highlights candidate driver genes |
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Relations |
BioProject |
PRJNA153911 |