Lucas Ogura Software Developer

Resume Projects Publications


  • Python, CSS, Javascript

Natural Language Analysis of emotions for Reddit comments

Check it out
Insight UBC
  • Typescript, Javascript, HTML, CSS, JQuery

Web application for searching course data from previous years or building/room information throughout campus.
Available soon on Heroku

Mind The Gap
  • Java

Android app for the London Tube. With the ability to visualize stations and train lines on a map, see timetables for every train and locate yourself to the nearest station.



Butcher, N. J., Merico, D., Zarrei, M., Ogura, L., Marshall, C. R., Chow, E. W., . . . Bassett, A. S. (2017). Whole-genome sequencing suggests mechanisms for 22q11.2 deletion-associated Parkinson’s disease. Plos One, 12(4). doi:10.1371/journal.pone.0173944

Costain, G., Lionel, A. C., Ogura, L., Marshall, C. R., Scherer, S. W., Silversides, C. K., Bassett, A. S. (2016). Genome-wide rare copy number variations contribute to genetic risk for transposition of the great arteries. International Journal of Cardiology, 204, 115-121. doi:10.1016/j.ijcard.2015.11.127

Merico, D., Zarrei, M., Costain, G., Ogura, L., Alipanahi, B., Gazzellone, M.J., Butcher, N.J., Thiruvahindrapuram, B., Nalpathamkalam, T., Chow, E.W., Andrade, D.M., Frey, B.J., Marshall, C.R., Scherer, S.W., Bassett, A.S. G3 (Bethesda). 2015 Sep 16;5(11):2453-61. doi: 10.1534/g3.115.021345.

Van, L., Butcher, N. J., Costain, G., Ogura, L., Chow, E. W., Bassett, A. S. (2015). Fetal growth and gestational factors as predictors of schizophrenia in 22q11.2 deletion syndrome. Genetics in Medicine, 18(4), 350-355. doi:10.1038/gim.2015.84

Chan, C., Costain, G., Ogura, L., Silversides, C. K., Chow, E. W., Bassett, A. S. (2015). Reproductive Health Issues for Adults with a Common Genomic Disorder: 22q11.2 Deletion Syndrome. Journal of Genetic Counseling, 24(5), 810-821. doi:10.1007/s10897-014-9811-7

Merico, D., Costain, G., Butcher, N. J., Warnica, W., Ogura, L., Alfred, S. E., . . . Bassett, A. S. (2014). MicroRNA Dysregulation, Gene Networks, and Risk for Schizophrenia in 22q11.2 Deletion Syndrome. Frontiers in Neurology, 5. doi:10.3389/fneur.2014.00238