SNPs Array Karyotyping in Non-Hodgkin Lymphoma
AbstractThe traditional methods for detection of chromosomal aberrations, which included cytogenetic or gene candidate solutions, suffered from low sensitivity or the need for previous knowledge of the target regions of the genome. With the advent of single nucleotide polymorphism (SNP) arrays, genome screening at global level in order to find chromosomal aberrations like copy number variants, DNA amplifications, deletions, and also loss of heterozygosity became feasible. In this review, we present an update of the knowledge, gained by SNPs arrays, of the genomic complexity of the most important subtypes of non-Hodgkin lymphomas. View Full-Text
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Etebari, M.; Navari, M.; Piccaluga, P.P. SNPs Array Karyotyping in Non-Hodgkin Lymphoma. Microarrays 2015, 4, 551-569.
Etebari M, Navari M, Piccaluga PP. SNPs Array Karyotyping in Non-Hodgkin Lymphoma. Microarrays. 2015; 4(4):551-569.Chicago/Turabian Style
Etebari, Maryam; Navari, Mohsen; Piccaluga, Pier P. 2015. "SNPs Array Karyotyping in Non-Hodgkin Lymphoma." Microarrays 4, no. 4: 551-569.