Bayesian copy number detection and association in large-scale studies

BACKGROUND: Germline copy number variants (CNVs) increase risk for many diseases, yet detection of CNVs and quantifying their contribution to disease risk in large-scale studies is challenging due to biological and technical sources of heterogeneity that vary across the genome within and between sam...

Volledige beschrijving

Bewaard in:
Bibliografische gegevens
Gepubliceerd in:BMC Cancer
Hoofdauteurs: Cristiano, Stephen, McKean, David, Carey, Jacob, Bracci, Paige, Brennan, Paul, Chou, Michael, Du, Mengmeng, Gallinger, Steven, Goggins, Michael G., Hassan, Manal M., Hung, Rayjean J., Kurtz, Robert C., Li, Donghui, Lu, Lingeng, Neale, Rachel, Olson, Sara, Petersen, Gloria, Rabe, Kari G., Fu, Jack, Risch, Harvey, Rosner, Gary L., Ruczinski, Ingo, Klein, Alison P., Scharpf, Robert B.
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: BioMed Central 2020
Onderwerpen:
Research Article
Online toegang:https://ncbi.nlm.nih.gov/pmc/articles/PMC7487704/
https://ncbi.nlm.nih.gov/pubmed/32894098
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12885-020-07304-3
Tags: Voeg label toe
Geen labels, Wees de eerste die dit record labelt!

Gelijkaardige items