Literature DB >> 14534186

Reconstructing tumor genome architectures.

Benjamin J Raphael1, Stanislav Volik, Colin Collins, Pavel A Pevzner.   

Abstract

Although cancer progression is often associated with genome rearrangements, little is known about the detailed genomic architecture of tumor genomes. The attempt to reconstruct the genomic organization of a tumor genome recently resulted in the development of the End Sequence Profiling (ESP) technique, and the application of this technique to human MCF7 tumor cells. We formulate the ESP Genome Reconstruction Problem, and develop an algorithm to solve this problem in the case of sparse ESP data. We apply our algorithm to analyze human MCF7 tumor cells, and obtain the first reconstruction of the putative architecture of human MCF7 tumor genome. Our results assist in the ongoing ESP analysis of MCF7 tumors by suggesting additional ESP experiments for the completion of a reliable reconstruction of the MCF7 tumor genome, and by focusing BAC re-sequencing efforts.

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Year:  2003        PMID: 14534186     DOI: 10.1093/bioinformatics/btg1074

Source DB:  PubMed          Journal:  Bioinformatics        ISSN: 1367-4803            Impact factor:   6.937


  33 in total

1.  Genome-wide mapping and assembly of structural variant breakpoints in the mouse genome.

Authors:  Aaron R Quinlan; Royden A Clark; Svetlana Sokolova; Mitchell L Leibowitz; Yujun Zhang; Matthew E Hurles; Joshua C Mell; Ira M Hall
Journal:  Genome Res       Date:  2010-03-22       Impact factor: 9.043

2.  Reconstructing cancer genomes from paired-end sequencing data.

Authors:  Layla Oesper; Anna Ritz; Sarah J Aerni; Ryan Drebin; Benjamin J Raphael
Journal:  BMC Bioinformatics       Date:  2012-04-19       Impact factor: 3.169

3.  Assessment of palindromes as platforms for DNA amplification in breast cancer.

Authors:  Jamie Guenthoer; Scott J Diede; Hisashi Tanaka; Xiaoyu Chai; Li Hsu; Stephen J Tapscott; Peggy L Porter
Journal:  Genome Res       Date:  2011-07-13       Impact factor: 9.043

Review 4.  Computational methods for discovering structural variation with next-generation sequencing.

Authors:  Paul Medvedev; Monica Stanciu; Michael Brudno
Journal:  Nat Methods       Date:  2009-11       Impact factor: 28.547

5.  Genomic Comparison of Two O111:H- Enterohemorrhagic Escherichia coli Isolates from a Historic Hemolytic-Uremic Syndrome Outbreak in Australia.

Authors:  Lauren J McAllister; Stephen J Bent; Nicola K Petty; Elizabeth Skippington; Scott A Beatson; James C Paton; Adrienne W Paton
Journal:  Infect Immun       Date:  2016-01-04       Impact factor: 3.441

6.  Pooled genomic indexing of rhesus macaque.

Authors:  Aleksandar Milosavljevic; Ronald A Harris; Erica J Sodergren; Andrew R Jackson; Ken J Kalafus; Anne Hodgson; Andrew Cree; Weilie Dai; Miklos Csuros; Baoli Zhu; Pieter J de Jong; George M Weinstock; Richard A Gibbs
Journal:  Genome Res       Date:  2005-02       Impact factor: 9.043

7.  Combinatorial algorithms for structural variation detection in high-throughput sequenced genomes.

Authors:  Fereydoun Hormozdiari; Can Alkan; Evan E Eichler; S Cenk Sahinalp
Journal:  Genome Res       Date:  2009-05-15       Impact factor: 9.043

8.  Reconstructing genome mixtures from partial adjacencies.

Authors:  Ahmad Mahmoody; Crystal L Kahn; Benjamin J Raphael
Journal:  BMC Bioinformatics       Date:  2012-12-19       Impact factor: 3.169

Review 9.  Expanding the computational toolbox for mining cancer genomes.

Authors:  Li Ding; Michael C Wendl; Joshua F McMichael; Benjamin J Raphael
Journal:  Nat Rev Genet       Date:  2014-07-08       Impact factor: 53.242

10.  A geometric approach for classification and comparison of structural variants.

Authors:  Suzanne Sindi; Elena Helman; Ali Bashir; Benjamin J Raphael
Journal:  Bioinformatics       Date:  2009-06-15       Impact factor: 6.937

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