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Dark matter RNA illuminates the puzzle of genome-wide association studies

In the past decade, numerous studies have made connections between sequence variants in human genomes and predisposition to complex diseases. However, most of these variants lie outside of the charted regions of the human genome whose function we understand; that is, the sequences that encode protei...

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Detalhes bibliográficos
Main Authors: St. Laurent, Georges, Vyatkin, Yuri, Kapranov, Philipp
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2014
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4054906/
https://ncbi.nlm.nih.gov/pubmed/24924000
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1741-7015-12-97
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