Clinical Application of Whole Genome Sequencing In Patients with Primary Immunodeficiency

This report illustrates the value of whole genome sequencing (WGS) in elucidating the genetic cause of disease in patients with primary immunodeficiency (PID). As sequencing costs decline, we predict that utilization of next generation sequencing (NGS) in the clinical setting will increase.

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Detalhes bibliográficos
Publicado no:J Allergy Clin Immunol
Main Authors: Mousallem, Talal, Urban, Thomas J., McSweeney, K. Melodi, Kleinstein, Sarah E., Zhu, Mingfu, Adeli, Mehdi, Parrott, Roberta E., Roberts, Joseph L., Krueger, Brian, Buckley, Rebecca H., Goldstein, David B
Formato: Artigo
Idioma:Inglês
Publicado em: 2015
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5037571/
https://ncbi.nlm.nih.gov/pubmed/25981738
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.jaci.2015.02.040
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