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note
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Acknowledgments: We thank A. Skrenchuk and B. Oskotsky (Stanford University) for computer support and E. Davydov, C. Do, S. Gross, and M. Schaub (Stanford University) for constructive discussion. Funding: This work was supported by Lucile Packard Foundation for Children's Health, the Hewlett Packard Foundation, National Institute of General Medical Sciences (R01 GM079719), National Cancer Institute (R01 CA138256), National Library of Medicine (T15 LM007033), Howard Hughes Medical Institute, and Pharmaceutical Research and Manufacturers of America Foundation. Author contributions: J.T.D., M. Sirota, and A.J.B. designed the study and carried out the analysis. M. Shenoy, M.M.S., R.K.P., S.R., and P.J.P. carried out validation experiments. A.A.M. and A.P.C. assisted in the analysis. J.T.D., M. Sirota, and A.J.B. wrote the paper. Competing interests: A.J.B. is on the scientific advisory board of NuMedii Inc. and Personalis and is a paid consultant for Lilly, Johnson and Johnson, Genstruct, Tercica, Ansh Labs, and Prevendia. J.T.D. is a consultant for NuMedii Inc. The other authors declare that they have no competing interests.
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