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Smoking + BMI in heart disease
WGS for cardiovascular outcomes
RNA-Seq in pancreatic cancer
Identifying the Genetic Explanation for Heritable Breast Cancer
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Selected Publications (1)
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FAVR (Filtering and Annotation of Variants that are Rare): methods to facilitate the analysis of rare germline genetic variants from massively parallel sequencing datasets
B. Pope, T. Nguyen-Dumont, F. Odefrey, et al. (2013). BMC Bioinformatics. Cited 13 times.
https://doi.org/10.1186/1471-2105-14-65
