CDG: An Online Server for Detecting Biologically Closest Disease-Causing Genes and its Application to Primary Immunodeficiency

High-throughput genomic technologies yield about 20,000 variants in the protein-coding exome of each individual. A commonly used approach to select candidate disease-causing variants is to test whether the associated gene has been previously reported to be disease-causing. In the absence of known di...

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Detalles Bibliográficos
Autores principales: Requena, David, Maffucci, Patrick, Bigio, Benedetta, Shang, Lei, Abhyankar, Avinash, Boisson, Bertrand, Stenson, Peter D., Cooper, David N., Cunningham-Rundles, Charlotte, Casanova, Jean-Laurent, Abel, Laurent, Itan, Yuval
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Immunology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6030251/
https://www.ncbi.nlm.nih.gov/pubmed/29997612
http://dx.doi.org/10.3389/fimmu.2018.01340

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6030251/
https://www.ncbi.nlm.nih.gov/pubmed/29997612
http://dx.doi.org/10.3389/fimmu.2018.01340

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