CNVrd, a Read-Depth Algorithm for Assigning Copy-Number at the FCGR Locus: Population-Specific Tagging of Copy Number Variation at FCGR3B

The extent of contribution from common gene copy number (CN) variants in human disease is currently unresolved. Part of the reason for this is the technical difficulty in directly measuring CN variation (CNV) using molecular methods, and the lack of single nucleotide polymorphisms (SNPs) that can ta...

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Detalles Bibliográficos
Autores principales: Nguyen, Hoang tan, Merriman, Tony R., Black, Michael A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3640002/
https://www.ncbi.nlm.nih.gov/pubmed/23646200
http://dx.doi.org/10.1371/journal.pone.0063219

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3640002/
https://www.ncbi.nlm.nih.gov/pubmed/23646200
http://dx.doi.org/10.1371/journal.pone.0063219

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