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Smoking + BMI in heart disease
WGS for cardiovascular outcomes
RNA-Seq in pancreatic cancer
Whole-genome sequencing in multiplex epilepsy families
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Overview
Selected Publications (4)
Variables (22)
The Characterization of Twenty Sequenced Human Genomes
Kimberly Pelak, K. Shianna, D. Ge, et al. (2010). PLoS Genetics. Cited 168 times.
https://doi.org/10.1371/journal.pgen.1001111
Using ERDS to infer copy-number variants in high-coverage genomes.
Mingfu Zhu, A. Need, Yujun Han, et al. (2012). American journal of human genetics. Cited 158 times.
https://doi.org/10.1016/j.ajhg.2012.07.004
Exome sequencing followed by large-scale genotyping fails to identify single rare variants of large effect in idiopathic generalized epilepsy.
E. Heinzen, C. Depondt, G. Cavalleri, et al. (2012). American journal of human genetics. Cited 110 times.
https://doi.org/10.1016/j.ajhg.2012.06.016
SVA: software for annotating and visualizing sequenced human genomes
D. Ge, E. Ruzzo, K. Shianna, et al. (2011). Bioinformatics. Cited 75 times.
https://doi.org/10.1093/bioinformatics/btr317
