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Detection and correction of artefacts in estimation of rare copy number variants and analysis of rare deletions in type 1 diabetes
Copy number variants (CNVs) have been proposed as a possible source of ‘missing heritability’ in complex human diseases. Two studies of type 1 diabetes (T1D) found null associations with common copy number polymorphisms, but CNVs of low frequency and high penetrance could still play a role. We used...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4381751/ https://www.ncbi.nlm.nih.gov/pubmed/25424174 http://dx.doi.org/10.1093/hmg/ddu581 |