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2019 | OriginalPaper | Buchkapitel

Parallel-Tempered Feature Allocation for Large-Scale Tumor Heterogeneity with Deep Sequencing Data

verfasst von : Yang Ni, Peter Müller, Max Shpak, Yuan Ji

Erschienen in: Pharmaceutical Statistics

Verlag: Springer International Publishing

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Abstract

We developed a parallel-tempered feature allocation algorithm to infer tumor heterogeneity from deep DNA sequencing data. The feature allocation model is based on a binomial likelihood and an Indian Buffet process prior on the latent haplotypes. A variation of parallel tempering technique is introduced to flatten peaked local modes of the posterior distribution, and yields a more efficient Markov chain Monte Carlo algorithm. Simulation studies provide empirical evidence that the proposed method is superior to competing methods at a high read depth. In our application to Glioblastoma multiforme data, we found several distinctive haplotypes that indicate the presence of multiple subclones in the tumor sample.

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Literatur
1.
Zurück zum Zitat Griffiths, T.L., Ghahramani, Z.: Infinite latent feature models and the indian buffet process. NIPS 18, 475–482 (2005) Griffiths, T.L., Ghahramani, Z.: Infinite latent feature models and the indian buffet process. NIPS 18, 475–482 (2005)
2.
Zurück zum Zitat Geyer, C.J.: Markov chain Monte Carlo maximum likelihood. In: Proceedings of the 23rd Symposium on the Interface, Computing Science and Statistics. Interface Foundation, Fairfax Station, VA (1991) Geyer, C.J.: Markov chain Monte Carlo maximum likelihood. In: Proceedings of the 23rd Symposium on the Interface, Computing Science and Statistics. Interface Foundation, Fairfax Station, VA (1991)
3.
Zurück zum Zitat Gerlinger, M., Rowan, A.J., Horswell, S., Larkin, J., Endesfelder, D., Gronroos, E., Martinez, P., Matthews, N., Stewart, A., Tarpey, P., et al.: Intratumor heterogeneity and branched evolution revealed by multiregion sequencing. N. Engl. J. Med. 2012(366), 883–892 (2012)CrossRef Gerlinger, M., Rowan, A.J., Horswell, S., Larkin, J., Endesfelder, D., Gronroos, E., Martinez, P., Matthews, N., Stewart, A., Tarpey, P., et al.: Intratumor heterogeneity and branched evolution revealed by multiregion sequencing. N. Engl. J. Med. 2012(366), 883–892 (2012)CrossRef
4.
Zurück zum Zitat Seoane, J., Mattos-Arruda, D., et al.: The challenge of intratumour heterogeneity in precision medicine. J. Intern. Med. 276(1), 41–51 (2014)CrossRef Seoane, J., Mattos-Arruda, D., et al.: The challenge of intratumour heterogeneity in precision medicine. J. Intern. Med. 276(1), 41–51 (2014)CrossRef
5.
Zurück zum Zitat De Bono, J., Ashworth, A.: Translating cancer research into targeted therapeutics. Nature 467(7315), 543–549 (2010)CrossRef De Bono, J., Ashworth, A.: Translating cancer research into targeted therapeutics. Nature 467(7315), 543–549 (2010)CrossRef
6.
Zurück zum Zitat Snyder, A., Makarov, V., Merghoub, T., Yuan, J., Zaretsky, J.M., Desrichard, A., Walsh, L.A., Postow, M.A., Wong, P., Ho, T.S., et al.: Genetic basis for clinical response to ctla-4 blockade in melanoma. N. Engl. J. Med. 371(23), 2189–2199 (2014)CrossRef Snyder, A., Makarov, V., Merghoub, T., Yuan, J., Zaretsky, J.M., Desrichard, A., Walsh, L.A., Postow, M.A., Wong, P., Ho, T.S., et al.: Genetic basis for clinical response to ctla-4 blockade in melanoma. N. Engl. J. Med. 371(23), 2189–2199 (2014)CrossRef
7.
Zurück zum Zitat Campbell, P.J., Pleasance, E.D., Stephens, P.J., Dicks, E., Rance, R., Goodhead, I., Follows, G.A., et al.: Subclonal phylogenetic structures in cancer revealed by ultra-deep sequencing. Proc. Natl. Acad. Sci. U. S. A. 105(35), 13,081–13,086 (2008)CrossRef Campbell, P.J., Pleasance, E.D., Stephens, P.J., Dicks, E., Rance, R., Goodhead, I., Follows, G.A., et al.: Subclonal phylogenetic structures in cancer revealed by ultra-deep sequencing. Proc. Natl. Acad. Sci. U. S. A. 105(35), 13,081–13,086 (2008)CrossRef
8.
Zurück zum Zitat Ling, S., Hu, Z., Yang, Z., Yang, F., Li, Y., Lin, P., Chen, K., Dong, L., Cao, L., Tao, Y., et al.: Extremely high genetic diversity in a single tumor points to prevalence of non-darwinian cell evolution. Proc. Natl. Acad. Sci. 112(47), E6496–E6505 (2015)CrossRef Ling, S., Hu, Z., Yang, Z., Yang, F., Li, Y., Lin, P., Chen, K., Dong, L., Cao, L., Tao, Y., et al.: Extremely high genetic diversity in a single tumor points to prevalence of non-darwinian cell evolution. Proc. Natl. Acad. Sci. 112(47), E6496–E6505 (2015)CrossRef
9.
Zurück zum Zitat Lee, J., Müller, P., Gulukota, K., Ji, Y., et al.: A bayesian feature allocation model for tumor heterogeneity. Ann/ Appl. Stat. 9(2), 621–639 (2015)MathSciNetCrossRef Lee, J., Müller, P., Gulukota, K., Ji, Y., et al.: A bayesian feature allocation model for tumor heterogeneity. Ann/ Appl. Stat. 9(2), 621–639 (2015)MathSciNetCrossRef
10.
Zurück zum Zitat Green, P.J.: Reversible jump markov chain Monte Carlo computation and Bayesian model determination. Biometrika 82(4), 711–732 (1995)MathSciNetCrossRef Green, P.J.: Reversible jump markov chain Monte Carlo computation and Bayesian model determination. Biometrika 82(4), 711–732 (1995)MathSciNetCrossRef
11.
Zurück zum Zitat O’Hagan, A.: Fractional Bayes factors for model comparison. J. R. Stat. Soc. Series B 57(1), 99–138 (1995)MathSciNetMATH O’Hagan, A.: Fractional Bayes factors for model comparison. J. R. Stat. Soc. Series B 57(1), 99–138 (1995)MathSciNetMATH
12.
Zurück zum Zitat Xu, Y., Müller, P., Yuan, Y., Gulukota, K., Ji, Y.: Mad bayes for tumor heterogeneity-feature allocation with exponential family sampling. J. Am. Stat. Assoc. 110(510), 503–514 (2015)MathSciNetCrossRef Xu, Y., Müller, P., Yuan, Y., Gulukota, K., Ji, Y.: Mad bayes for tumor heterogeneity-feature allocation with exponential family sampling. J. Am. Stat. Assoc. 110(510), 503–514 (2015)MathSciNetCrossRef
13.
Zurück zum Zitat Dahl, D.B.: Model-based clustering for expression data via a Dirichlet process mixture model. In: Bayesian Inference for Gene Expression and Proteomics, pp. 201–218 (2006) Dahl, D.B.: Model-based clustering for expression data via a Dirichlet process mixture model. In: Bayesian Inference for Gene Expression and Proteomics, pp. 201–218 (2006)
14.
Zurück zum Zitat Sottoriva, A., Spiteri, I., Piccirillo, S.G., Touloumis, A., Collins, V.P., Marioni, J.C., Curtis, C., Watts, C., Tavaré, S.: Intratumor heterogeneity in human glioblastoma reflects cancer evolutionary dynamics. Proc. Natl. Acad. Sci. 110(10), 4009–4014 (2013)CrossRef Sottoriva, A., Spiteri, I., Piccirillo, S.G., Touloumis, A., Collins, V.P., Marioni, J.C., Curtis, C., Watts, C., Tavaré, S.: Intratumor heterogeneity in human glioblastoma reflects cancer evolutionary dynamics. Proc. Natl. Acad. Sci. 110(10), 4009–4014 (2013)CrossRef
15.
Zurück zum Zitat McKenna, A., Hanna, M., Banks, E., Sivachenko, A., Cibulskis, K., Kernytsky, A., Garimella, K., Altshuler, D., Gabriel, S., Daly, M., et al.: The genome analysis toolkit: a mapreduce framework for analyzing next-generation dna sequencing data. Genome Res. 20(9), 1297–1303 (2010)CrossRef McKenna, A., Hanna, M., Banks, E., Sivachenko, A., Cibulskis, K., Kernytsky, A., Garimella, K., Altshuler, D., Gabriel, S., Daly, M., et al.: The genome analysis toolkit: a mapreduce framework for analyzing next-generation dna sequencing data. Genome Res. 20(9), 1297–1303 (2010)CrossRef
16.
Zurück zum Zitat DePristo, M.A., Banks, E., Poplin, R., Garimella, K.V., Maguire, J.R., Hartl, C., Philippakis, A.A., Del Angel, G., Rivas, M.A., Hanna, M., et al.: A framework for variation discovery and genotyping using next-generation DNA sequencing data. Nat. Genet. 43(5), 491–498 (2011)CrossRef DePristo, M.A., Banks, E., Poplin, R., Garimella, K.V., Maguire, J.R., Hartl, C., Philippakis, A.A., Del Angel, G., Rivas, M.A., Hanna, M., et al.: A framework for variation discovery and genotyping using next-generation DNA sequencing data. Nat. Genet. 43(5), 491–498 (2011)CrossRef
17.
Zurück zum Zitat Auwera, G.A., Carneiro, M.O., Hartl, C., Poplin, R., del Angel, G., Levy-Moonshine, A., Jordan, T., Shakir, K., Roazen, D., Thibault, J., et al.: From FASTQ data to high-confidence variant calls: the genome analysis toolkit best practices pipeline. In: Current Protocols in Bioinformatics, pp. 11.10.1–11.10.33 (2013) Auwera, G.A., Carneiro, M.O., Hartl, C., Poplin, R., del Angel, G., Levy-Moonshine, A., Jordan, T., Shakir, K., Roazen, D., Thibault, J., et al.: From FASTQ data to high-confidence variant calls: the genome analysis toolkit best practices pipeline. In: Current Protocols in Bioinformatics, pp. 11.10.1–11.10.33 (2013)
18.
Zurück zum Zitat Qiao, W., Quon, G., Csaszar, E., Yu, M., Morris, Q., Zandstra, P.W.: Pert: a method for expression deconvolution of human blood samples from varied microenvironmental and developmental conditions. PLoS Comput. Biol. 8(12), e1002, 838 (2012)CrossRef Qiao, W., Quon, G., Csaszar, E., Yu, M., Morris, Q., Zandstra, P.W.: Pert: a method for expression deconvolution of human blood samples from varied microenvironmental and developmental conditions. PLoS Comput. Biol. 8(12), e1002, 838 (2012)CrossRef
19.
Zurück zum Zitat Ahn, J., Yuan, Y., Parmigiani, G., Suraokar, M.B., Diao, L., Wistuba, I.I., Wang, W.: Demix: deconvolution for mixed cancer transcriptomes using raw measured data. Bioinformatics (2013) Ahn, J., Yuan, Y., Parmigiani, G., Suraokar, M.B., Diao, L., Wistuba, I.I., Wang, W.: Demix: deconvolution for mixed cancer transcriptomes using raw measured data. Bioinformatics (2013)
20.
Zurück zum Zitat Ren, B., Bacallado, S., Favaro, S., Vatanen, T., Huttenhower, C., Trippa, L.: Bayesian nonparametric mixed effects models in microbiome data analysis. arXiv:1711.01241 (2017) Ren, B., Bacallado, S., Favaro, S., Vatanen, T., Huttenhower, C., Trippa, L.: Bayesian nonparametric mixed effects models in microbiome data analysis. arXiv:​1711.​01241 (2017)
Metadaten
Titel
Parallel-Tempered Feature Allocation for Large-Scale Tumor Heterogeneity with Deep Sequencing Data
verfasst von
Yang Ni
Peter Müller
Max Shpak
Yuan Ji
Copyright-Jahr
2019
DOI
https://doi.org/10.1007/978-3-319-67386-8_17