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RNA-Seq and human complex diseases: recent accomplishments and future perspectives

The availability of the human genome sequence has allowed identification of disease-causing mutations in many Mendelian disorders, and detection of significant associations of nucleotide polymorphisms to complex diseases and traits. Despite these progresses, finding the causative variations for most...

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Detalhes bibliográficos
Main Authors: Costa, Valerio, Aprile, Marianna, Esposito, Roberta, Ciccodicola, Alfredo
Formato: Artigo
Idioma:Inglês
Publicado em: Nature Publishing Group 2013
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3548270/
https://ncbi.nlm.nih.gov/pubmed/22739340
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/ejhg.2012.129
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