CNstream: A method for the identification and genotyping of copy number polymorphisms using Illumina microarrays

BACKGROUND: Understanding the genetic basis of disease risk in depth requires an exhaustive knowledge of the types of genetic variation. Very recently, Copy Number Variants (CNVs) have received much attention because of their potential implication in common disease susceptibility. Copy Number Polymo...

Ful tanımlama

Kaydedildi:
Detaylı Bibliyografya
Asıl Yazarlar: Alonso, Arnald, Julià, Antonio, Tortosa, Raül, Canaleta, Cristina, Cañete, Juan D, Ballina, Javier, Balsa, Alejandro, Tornero, Jesús, Marsal, Sara
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: BioMed Central 2010
Konular:
Methodology Article
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC3098064/
https://ncbi.nlm.nih.gov/pubmed/20482829
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2105-11-264
Etiketler: Etiketle
Etiket eklenmemiş, İlk siz ekleyin!

Benzer Materyaller