A Linear-Time Algorithm for the Copy Number Transformation Problem
暂无分享,去创建一个
[1] Denis Bertrand,et al. Genome Halving and Double Distance with Losses , 2011, J. Comput. Biol..
[2] Russell Schwartz,et al. Inferring models of multiscale copy number evolution for single-tumor phylogenetics , 2015, Bioinform..
[3] Guillaume Fertin,et al. Combinatorics of Genome Rearrangements , 2009, Computational molecular biology.
[4] Benjamin J. Raphael,et al. Integrated Genomic Analyses of Ovarian Carcinoma , 2011, Nature.
[5] J W Gray,et al. Cytogenetic analysis using quantitative, high-sensitivity, fluorescence hybridization. , 1986, Proceedings of the National Academy of Sciences of the United States of America.
[6] Benjamin J. Raphael,et al. Reconstructing cancer genomes from paired-end sequencing data , 2012, BMC Bioinformatics.
[7] Mehryar Mohri. Weighted Finite-State Transducer Algorithms. An Overview , 2004 .
[8] James D. Brenton,et al. Phylogenetic Quantification of Intra-tumour Heterogeneity , 2013, PLoS Comput. Biol..
[9] Alexander Eckehart Urban,et al. High-resolution mapping of DNA copy alterations in human chromosome 22 using high-density tiling oligonucleotide arrays. , 2006, Proceedings of the National Academy of Sciences of the United States of America.
[10] W. Hahn,et al. BreaKmer: detection of structural variation in targeted massively parallel sequencing data using kmers , 2014, Nucleic acids research.
[11] E. Letouzé,et al. Analysis of the copy number profiles of several tumor samples from the same patient reveals the successive steps in tumorigenesis , 2010, Genome Biology.
[12] Russell Schwartz,et al. Phylogenetic analysis of multiprobe fluorescence in situ hybridization data from tumor cell populations , 2013, Bioinform..
[13] Yu Lin,et al. Approximating the edit distance for genomes with duplicate genes under DCJ, insertion and deletion , 2012, BMC Bioinformatics.
[14] Mehryar Mohri. Edit-Distance Of Weighted Automata: General Definitions And Algorithms , 2003, Int. J. Found. Comput. Sci..
[15] Russell Schwartz,et al. Algorithms to Model Single Gene, Single Chromosome, and Whole Genome Copy Number Changes Jointly in Tumor Phylogenetics , 2014, PLoS Comput. Biol..
[16] S. C. Sahinalp,et al. nFuse: Discovery of complex genomic rearrangements in cancer using high-throughput sequencing , 2012, Genome research.
[17] David Sankoff,et al. Multichromosomal median and halving problems under different genomic distances , 2009, BMC Bioinformatics.