|
Status |
Public on Aug 07, 2013 |
Title |
Next-generation sequencing of cancers of unknown primary (Affymetrix GenomeWideSNP data) |
Organism |
Homo sapiens |
Experiment type |
Genome variation profiling by SNP array SNP genotyping by SNP array
|
Summary |
SNP 6.0 copy number analysis was done to validate results from next-generation sequencing read-depth CNV analysis in a cohort of cancers of unknown primary
|
|
|
Overall design |
Affymetrix SNP arrays were performed according to the manufacturer's directions on DNA extracted from cryopreserved tissue samples 7 samples
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Contributor(s) |
Tothill R, Cowin P, Bowtell D |
Citation(s) |
24037760 |
Submission date |
Aug 06, 2013 |
Last update date |
Nov 27, 2018 |
Contact name |
Richard William Tothill |
E-mail(s) |
richard.tothill@petermac.org
|
Organization name |
Peter MacCallum Cancer Centre
|
Department |
Research
|
Lab |
Molecular Genomics
|
Street address |
St Andrews Place
|
City |
Melbourne |
State/province |
Victoria |
ZIP/Postal code |
3001 |
Country |
Australia |
|
|
Platforms (1) |
GPL6801 |
[GenomeWideSNP_6] Affymetrix Genome-Wide Human SNP 6.0 Array |
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Samples (7)
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Relations |
BioProject |
PRJNA214423 |