I currently work at Personalis, where I lead our bioinformatics science efforts, focusing on developing computational solutions to analyze cancer samples using next-generation sequencing technology. My team’s work includes determining appropriate sequencing protocols, designing and developing novel immuno-oncology tools, and profiling/interpreting cancer patient samples. I previously worked in personalized genomic medicine at Stanford University where I identified causal genomic variants for diseases in individuals and families, including cancer and rare mendelian disease.Specialties: Personalized genomic medicine, cancer genomic interpretation, whole-genome sequencing, exome sequencing, RNA-seq, personal genome annotation, genomic variant-drug associations, cancer gene driver identification, ligand prediction, chemical structure analysis, insect and mammalian olfaction, neuroscience, protein-protein interactions, human diseases, image analysis.
Listed skills include Bioinformatics, Molecular Biology, Computational Biology, Neuroscience, and 19 others.