Identifying rare and common disease associated variants in genomic data using Parkinson’s disease as a model

BACKGROUND: Genome-wide association studies have been successful in identifying common genetic variants for human diseases. However, much of the heritable variation associated with diseases such as Parkinson’s disease remains unknown suggesting that many more risk loci are yet to be identified. Rare...

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Detalles Bibliográficos
Autores principales: Lin, Ying-Chao, Hsieh, Ai-Ru, Hsiao, Ching-Lin, Wu, Shang-Jung, Wang, Hui-Min, Lian, Ie-Bin, Fann, Cathy SJ
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4428531/
https://www.ncbi.nlm.nih.gov/pubmed/25175702
http://dx.doi.org/10.1186/s12929-014-0088-9

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4428531/
https://www.ncbi.nlm.nih.gov/pubmed/25175702
http://dx.doi.org/10.1186/s12929-014-0088-9

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