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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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| Autors principals: | , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Nature Publishing Group
2013
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| Matèries: | |
| Accés en línia: | 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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