Understanding mutational effects in digenic diseases

To further our understanding of the complexity and genetic heterogeneity of rare diseases, it has become essential to shed light on how combinations of variants in different genes are responsible for a disease phenotype. With the appearance of a resource on digenic diseases, it has become possible t...

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Veröffentlicht in:	Nucleic acids research 2017-09, Vol.45 (15), p.e140-e140
Hauptverfasser:	Gazzo, Andrea, Raimondi, Daniele, Daneels, Dorien, Moreau, Yves, Smits, Guillaume, Van Dooren, Sonia, Lenaerts, Tom
Format:	Artikel
Sprache:	eng
Schlagworte:	Computational Biology - methods Datasets as Topic Epistasis, Genetic - physiology Genetic Association Studies - methods Genetic Diseases, Inborn - diagnosis Genetic Diseases, Inborn - genetics Genetic Predisposition to Disease Humans Methods Online Models, Genetic Mutation - physiology Phenotype Prognosis Validation Studies as Topic
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