Normalization of whole-genome SNP data from non-Hodgkin lymphoma patients for copy number variation.
Source: NCBI BioProject (ID PRJNA205289)
Source: NCBI BioProject (ID PRJNA205289)
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Project name: Homo sapiens
Description: With the whole genome SNPs array information, we could evaluate the copy number variation of samples so as to find out specific DNA aberrations in non-Hodgkin lymphma comparing with reactive hyperplasia patients.Overall design: To find out lymphoma-related copy number variations in 45 non-Hodgkin lymphoma patients comparing with 8 reactive hyperplasia patients.
Data type: Variation
Sample scope: Multiisolate
Relevance: Medical
Organization: Shanghai Institute of Hematology
Literatures
- PMID: 24586676
Last updated: 2013-05-24