Does Relaxing the Infinite Sites Assumption Give Better Tumor Phylogenies? An ILP-Based Comparative Approach
暂无分享,去创建一个
[1] Nilgun Donmez,et al. Clonality inference in multiple tumor samples using phylogeny , 2015, Bioinform..
[2] K. Kinzler,et al. Cancer Genome Landscapes , 2013, Science.
[3] Dan Gusfield,et al. Persistent phylogeny: a galled-tree and integer linear programming approach , 2015, BCB.
[4] Steven A. Roberts,et al. Mutational heterogeneity in cancer and the search for new cancer-associated genes , 2013 .
[5] M. Steel. The complexity of reconstructing trees from qualitative characters and subtrees , 1992 .
[6] Paola Bonizzoni,et al. The binary perfect phylogeny with persistent characters , 2011, Theor. Comput. Sci..
[7] Shankar Vembu,et al. PhyloWGS: Reconstructing subclonal composition and evolution from whole-genome sequencing of tumors , 2015, Genome Biology.
[8] Dan Gusfield. Algorithms on Strings, Trees, and Sequences - Computer Science and Computational Biology , 1997 .
[9] Benjamin J. Raphael,et al. Inferring the Mutational History of a Tumor Using Multi-state Perfect Phylogeny Mixtures. , 2016, Cell systems.
[10] Mike A. Steel,et al. Phylogeny - discrete and random processes in evolution , 2016, CBMS-NSF regional conference series in applied mathematics.
[11] Benjamin J. Raphael,et al. Advances for studying clonal evolution in cancer. , 2013, Cancer letters.
[12] Jenny Taylor,et al. Monitoring chronic lymphocytic leukemia progression by whole genome sequencing reveals heterogeneous clonal evolution patterns. , 2012, Blood.
[13] Benjamin J. Raphael,et al. Reconstruction of clonal trees and tumor composition from multi-sample sequencing data , 2015, Bioinform..
[14] N. Navin. Cancer genomics: one cell at a time , 2014, Genome Biology.
[15] Dan Gusfield,et al. Efficient algorithms for inferring evolutionary trees , 1991, Networks.
[16] J. Farris. Phylogenetic Analysis Under Dollo's Law , 1977 .
[17] Nancy R. Zhang,et al. Assessing intratumor heterogeneity and tracking longitudinal and spatial clonal evolutionary history by next-generation sequencing , 2016, Proceedings of the National Academy of Sciences.
[18] Dumitru Brinza,et al. An integer programming approach to novel transcript reconstruction from paired-end RNA-Seq reads , 2012, BCB.
[19] Shankar Vembu,et al. Inferring clonal evolution of tumors from single nucleotide somatic mutations , 2012, BMC Bioinformatics.
[20] Richard R. Hudson,et al. Generating samples under a Wright-Fisher neutral model of genetic variation , 2002, Bioinform..
[21] Faraz Hach,et al. CLIIQ: Accurate Comparative Detection and Quantification of Expressed Isoforms in a Population , 2012, WABI.
[22] R. Sokal,et al. A METHOD FOR DEDUCING BRANCHING SEQUENCES IN PHYLOGENY , 1965 .
[23] Jack Kuipers,et al. Tree inference for single-cell data , 2016 .
[24] Dannie Durand,et al. Graph Theoretical Insights into Evolution of Multidomain Proteins , 2005, RECOMB.
[25] Ron Shamir,et al. Incomplete Directed Perfect Phylogeny , 2000, CPM.
[26] P. A. Futreal,et al. Genomic architecture and evolution of clear cell renal cell carcinomas defined by multiregion sequencing , 2014, Nature Genetics.
[27] Jack Kuipers,et al. Single-cell sequencing data reveal widespread recurrence and loss of mutational hits in the life histories of tumors , 2017, Genome research.
[28] Paola Bonizzoni,et al. A colored graph approach to perfect phylogeny with persistent characters , 2017, Theor. Comput. Sci..
[29] Daniel G. Brown,et al. Integer Programming Formulations and Computations Solving Phylogenetic and Population Genetic Problems with Missing or Genotypic Data , 2007, COCOON.
[30] Paola Bonizzoni,et al. When and How the Perfect Phylogeny Model Explains Evolution , 2014, Discrete and Topological Models in Molecular Biology.
[31] Iman Hajirasouliha,et al. A combinatorial approach for analyzing intra-tumor heterogeneity from high-throughput sequencing data , 2014, Bioinform..
[32] Paola Bonizzoni,et al. Explaining evolution via constrained persistent perfect phylogeny , 2014, BMC Genomics.
[33] L. Michaux,et al. 14q deletions are associated with trisomy 12, NOTCH1 mutations and unmutated IGHV genes in chronic lymphocytic leukemia and small lymphocytic lymphoma , 2014, Genes, chromosomes & cancer.
[34] Carlo C. Maley,et al. Clonal evolution in cancer , 2012, Nature.