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Copy number variations and cancer

DNA copy number variations (CNVs) are an important component of genetic variation, affecting a greater fraction of the genome than single nucleotide polymorphisms (SNPs). The advent of high-resolution SNP arrays has made it possible to identify CNVs. Characterization of widespread constitutional (ge...

Täydet tiedot

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Bibliografiset tiedot
Päätekijät: Shlien, Adam, Malkin, David
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: BioMed Central 2009
Aiheet:
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC2703871/
https://ncbi.nlm.nih.gov/pubmed/19566914
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/gm62
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