Working toward precision medicine: Predicting phenotypes from exomes in the Critical Assessment of Genome Interpretation (CAGI) challenges.

Printer-friendly versionPrinter-friendly versionPDF versionPDF version
TitleWorking toward precision medicine: Predicting phenotypes from exomes in the Critical Assessment of Genome Interpretation (CAGI) challenges.
Publication TypeJournal Article
Year of Publication2017
AuthorsDaneshjou, R, Wang, Y, Bromberg, Y, Bovo, S, Martelli, PL, Babbi, G, Di Lena, P, Casadio, R, Edwards, M, Gifford, D, Jones, DT, Sundaram, L, Bhat, R, Li, X, Pal, LR, Kundu, K, Yin, Y, Moult, J, Jiang, Y, Pejaver, V, Pagel, KA, Li, B, Mooney, SD, Radivojac, P, Shah, S, Carraro, M, Gasparini, A, Leonardi, E, Giollo, M, Ferrari, C, Tosatto, SCE, Bachar, E, Azaria, JR, Ofran, Y, Unger, R, Niroula, A, Vihinen, M, Chang, B, Wang, MH, Franke, A, Petersen, B-S, Pirooznia, M, Zandi, P, McCombie, R, Potash, JB, Altman, RB, Klein, TE, Hoskins, RA, Repo, S, Brenner, SE, Morgan, AA
JournalHum Mutat
Date Published2017 Jun 21
ISSN1098-1004
Abstract

Precision medicine aims to predict a patient's disease risk and best therapeutic options by using that individual's genetic sequencing data. The Critical Assessment of Genome Interpretation (CAGI) is a community experiment consisting of genotype-phenotype prediction challenges; participants build models, undergo assessment, and share key findings. For CAGI 4, three challenges involved using exome-sequencing data: Crohn's disease, bipolar disorder, and warfarin dosing. Previous CAGI challenges included prior versions of the Crohn's disease challenge. Here, we discuss the range of techniques used for phenotype prediction as well as the methods used for assessing predictive models. Additionally, we outline some of the difficulties associated with making predictions and evaluating them. The lessons learned from the exome challenges can be applied to both research and clinical efforts to improve phenotype prediction from genotype. In addition, these challenges serve as a vehicle for sharing clinical and research exome data in a secure manner with scientists who have a broad range of expertise, contributing to a collaborative effort to advance our understanding of genotype-phenotype relationships.

DOI10.1002/humu.23280
Alternate JournalHum. Mutat.
PubMed ID28634997
Grant ListR13 HG006650 / HG / NHGRI NIH HHS / United States
U41 HG007346 / HG / NHGRI NIH HHS / United States