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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Shranjeno v:
Bibliografske podrobnosti
izdano v:J Biomed Sci
Main Authors: Lin, Ying-Chao, Hsieh, Ai-Ru, Hsiao, Ching-Lin, Wu, Shang-Jung, Wang, Hui-Min, Lian, Ie-Bin, Fann, Cathy SJ
Format: Artigo
Jezik:Inglês
Izdano: BioMed Central 2014
Teme:
Research
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC4428531/
https://ncbi.nlm.nih.gov/pubmed/25175702
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12929-014-0088-9
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