TY - JOUR
T1 - Prediction of human population responses to toxic compounds by a collaborative competition
AU - Eduati, Federica
AU - Mangravite, Lara M.
AU - Wang, Tao
AU - Tang, Hao
AU - Bare, J. Christopher
AU - Huang, Ruili
AU - Norman, Thea
AU - Kellen, Mike
AU - Menden, Michael P.
AU - Yang, Jichen
AU - Zhan, Xiaowei
AU - Zhong, Rui
AU - Xiao, Guanghua
AU - Xia, Menghang
AU - Abdo, Nour
AU - Kosyk, Oksana
AU - Friend, Stephen
AU - Dearry, Allen
AU - Simeonov, Anton
AU - Tice, Raymond R.
AU - Rusyn, Ivan
AU - Wright, Fred A.
AU - Stolovitzky, Gustavo
AU - Xie, Yang
AU - Saez-Rodriguez, Julio
AU - Aittokallio, Tero
AU - Alaimo, Salvatore
AU - Amadoz, Alicia
AU - Ammad-ud-din, Muhammad
AU - Azencott, Chloé Agathe
AU - Bacardit, Jaume
AU - Barron, Pelham
AU - Bernard, Elsa
AU - Beyer, Andreas
AU - Bin, Shao
AU - van Bömmel, Alena
AU - Borgwardt, Karsten
AU - Brys, April M.
AU - Caffrey, Brian
AU - Chang, Jeffrey
AU - Chang, Jungsoo
AU - Chheda, Himanshu
AU - Christodoulou, Eleni G.
AU - Clément-Ziza, Mathieu
AU - Cohen, Trevor
AU - Cowherd, Marianne
AU - Demeyer, Sofie
AU - Dopazo, Joaquin
AU - Elhard, Joel D.
AU - Kaski, Samuel
AU - the NIEHS-NCATS-UNC DREAM Toxicogenetics Collaboration
PY - 2015/9/10
Y1 - 2015/9/10
N2 - The ability to computationally predict the effects of toxic compounds on humans could help address the deficiencies of current chemical safety testing. Here, we report the results from a community-based DREAM challenge to predict toxicities of environmental compounds with potential adverse health effects for human populations. We measured the cytotoxicity of 156 compounds in 884 lymphoblastoid cell lines for which genotype and transcriptional data are available as part of the Tox21 1000 Genomes Project. The challenge participants developed algorithms to predict interindividual variability of toxic response from genomic profiles and population-level cytotoxicity data from structural attributes of the compounds. 179 submitted predictions were evaluated against an experimental data set to which participants were blinded. Individual cytotoxicity predictions were better than random, with modest correlations (Pearson's r < 0.28), consistent with complex trait genomic prediction. In contrast, predictions of population-level response to different compounds were higher (r < 0.66). The results highlight the possibility of predicting health risks associated with unknown compounds, although risk estimation accuracy remains suboptimal.
AB - The ability to computationally predict the effects of toxic compounds on humans could help address the deficiencies of current chemical safety testing. Here, we report the results from a community-based DREAM challenge to predict toxicities of environmental compounds with potential adverse health effects for human populations. We measured the cytotoxicity of 156 compounds in 884 lymphoblastoid cell lines for which genotype and transcriptional data are available as part of the Tox21 1000 Genomes Project. The challenge participants developed algorithms to predict interindividual variability of toxic response from genomic profiles and population-level cytotoxicity data from structural attributes of the compounds. 179 submitted predictions were evaluated against an experimental data set to which participants were blinded. Individual cytotoxicity predictions were better than random, with modest correlations (Pearson's r < 0.28), consistent with complex trait genomic prediction. In contrast, predictions of population-level response to different compounds were higher (r < 0.66). The results highlight the possibility of predicting health risks associated with unknown compounds, although risk estimation accuracy remains suboptimal.
UR - http://www.scopus.com/inward/record.url?scp=84941076570&partnerID=8YFLogxK
U2 - 10.1038/nbt.3299
DO - 10.1038/nbt.3299
M3 - Article
C2 - 26258538
AN - SCOPUS:84941076570
SN - 1087-0156
VL - 33
SP - 933
EP - 940
JO - NATURE BIOTECHNOLOGY
JF - NATURE BIOTECHNOLOGY
IS - 9
ER -