Reducing the exome search space for Mendelian diseases using genetic linkage analysis of exome genotypes

Many exome sequencing studies of Mendelian disorders fail to optimally exploit family information. Classical genetic linkage analysis is an effective method for eliminating a large fraction of the candidate causal variants discovered, even in small families that lack a unique linkage peak. We demons...

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Detalles Bibliográficos
Autores principales: Smith, Katherine R, Bromhead, Catherine J, Hildebrand, Michael S, Shearer, A Eliot, Lockhart, Paul J, Najmabadi, Hossein, Leventer, Richard J, McGillivray, George, Amor, David J, Smith, Richard J, Bahlo, Melanie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Method
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3308048/
https://www.ncbi.nlm.nih.gov/pubmed/21917141
http://dx.doi.org/10.1186/gb-2011-12-9-r85

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3308048/
https://www.ncbi.nlm.nih.gov/pubmed/21917141
http://dx.doi.org/10.1186/gb-2011-12-9-r85

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