Mapping the genotype-phenotype relationship in complex disease.


Autoria(s): MOHANASUNDARAM, KAAVYA
Contribuinte(s)

Wouters, Merridee

Crowley Tamsyn

Data(s)

01/04/2016

Resumo

Computational methods to identify harmful variations in humans perform well for rare diseases such as Huntington's but not for common diseases like hypertension or diabetes. A modelling approach that takes protein context into account was illustrated to identify harmful variants involved in complex diseases.

Identificador

http://hdl.handle.net/10536/DRO/DU:30089160

Idioma(s)

eng

Publicador

Deakin University, Faculty of Health, School of Medicine

Relação

http://dro.deakin.edu.au/eserv/DU:30089160/Mohanasundaram-agreement-2016.pdf

http://dro.deakin.edu.au/eserv/DU:30089160/Mohanasundaram-mappingthe-2016A.pdf

Direitos

The Author. All Rights Reserved

Palavras-Chave #Bioinformatics #Genetics #Diseases #Mendelian disease
Tipo

Thesis