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Status |
Public on Apr 17, 2019 |
Title |
Single nucleotide variants (SNVs) associated with cutaneous melanoma (CM) risk and prognosis |
Organism |
Homo sapiens |
Experiment type |
SNP genotyping by SNP array Genome variation profiling by SNP array
|
Summary |
Abnormalities in pigmentation-related genes alter CM risk and prognosis.
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Overall design |
Two hundred and six individuals were analyzed in the first stage. Genomic DNA was extracted from leukocytes of peripheral blood of 103 CM patients and 103 controls using the QIAamp DNA Blood Midi Kit (Qiagen®, Canada), following manufacturer’s instructions
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Contributor(s) |
Oliveira C, Lourenço GJ, Leme CS |
Citation(s) |
32699307 |
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Submission date |
Apr 16, 2019 |
Last update date |
Jul 27, 2020 |
Contact name |
Benilton Sa Carvalho |
Organization name |
Universidade Estadual de Campinas
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Department |
Medical Genetics
|
Lab |
Bioinformatics
|
Street address |
Tessália Vieira de Camargo, 126
|
City |
Campinas |
State/province |
Sao Paulo |
ZIP/Postal code |
13083887 |
Country |
Brazil |
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Platforms (1) |
GPL6801 |
[GenomeWideSNP_6] Affymetrix Genome-Wide Human SNP 6.0 Array |
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Samples (206)
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Relations |
BioProject |
PRJNA533122 |