Developing methods for the analysis of massively parallel sequencing data in family studies [ 2010 - 2014 ]

Research Grant

Researchers Bahlo Dr Melanie

Brief description This project will develop analytical methods to use the latest, high-throughput method of generating sequencing data, i.e. the letters of the human genome alphabet. These tools will be used to identify the causal mutations in families with inherited disorders, leading to diagnostic tests for these families.

Funding Amount $699,512

Funding Scheme Future Fellowships