I am a Masters student in the Computer Science department at Stanford University, as well as a research assistant in the Bejerano Lab. My interests include a variety of topics that lie within the intersection of computer science, biology, and medicine, such as rare genetic variation, the heritability of complex disease, and regulatory genomics.

In 2016, I received a B.S. in Computer Science, with honors, from Stanford University. Before my work in genomics, I worked as a production assistant at Four Directions Productions. I also worked as a software engineer for the Python Software Foundation, Yahoo! Research - Latin America, and Facebook.


Publications

M-CAP eliminates majority of variants of uncertain significance in clinical exomes at 95% sensitivity
Karthik A. Jagadeesh*, Aaron M. Wenger*, Mark J. Berger, Harendra Guturu, Peter D. Stenson, David N. Cooper, Jonathan A. Bernstein, Gill Bejerano
To appear in Nature Genetics

Research Experience

Curtis Lab, April 2016 - September 2016

In the Curtis Lab, I studied a subtype of breast cancer using next-generation sequencing technologies. This included a wide variety of methods, including whole-genome sequencing, copy number assays, and RNA-seq.

Bejerano Lab, April 2015 - June 2016

In the Bejerano Lab, I worked on tools which help research scientists and clinical geneticists diagnose patients with rare genetic diseases. Oftentimes, doctors cannot properly diagnose a child with rare genetic defects. Therefore, the doctor will sequence the protein-coding portion of the child's DNA to see if the patient harbors any known disease-causing mutations. If the child does not carry a known disease-causing mutation, the clinician must examine a list of 300 to 500 variants which might be causing the disease. During my time in the Bejerano Lab, I worked on tools which help to reduce this list of uncertain variants.