Literature DB >> 26578606

BubbleTree: an intuitive visualization to elucidate tumoral aneuploidy and clonality using next generation sequencing data.

Wei Zhu1, Michael Kuziora2, Todd Creasy2, Zhongwu Lai3, Christopher Morehouse2, Xiang Guo4, Yinong Sebastian2, Dong Shen2, Jiaqi Huang2, Jonathan R Dry3, Feng Xue5, Liyan Jiang6, Yihong Yao2, Brandon W Higgs1.   

Abstract

Tumors are characterized by properties of genetic instability, heterogeneity, and significant oligoclonality. Elucidating this intratumoral heterogeneity is challenging but important. In this study, we propose a framework, BubbleTree, to characterize the tumor clonality using next generation sequencing (NGS) data. BubbleTree simultaneously elucidates the complexity of a tumor biopsy, estimating cancerous cell purity, tumor ploidy, allele-specific copy number, and clonality and represents this in an intuitive graph. We further developed a three-step heuristic method to automate the interpretation of the BubbleTree graph, using a divide-and-conquer strategy. In this study, we demonstrated the performance of BubbleTree with comparisons to similar commonly used tools such as THetA2, ABSOLUTE, AbsCN-seq and ASCAT, using both simulated and patient-derived data. BubbleTree outperformed these tools, particularly in identifying tumor subclonal populations and polyploidy. We further demonstrated BubbleTree's utility in tracking clonality changes from patients' primary to metastatic tumor and dating somatic single nucleotide and copy number variants along the tumor clonal evolution. Overall, the BubbleTree graph and corresponding model is a powerful approach to provide a comprehensive spectrum of the heterogeneous tumor karyotype in human tumors. BubbleTree is R-based and freely available to the research community (https://www.bioconductor.org/packages/release/bioc/html/BubbleTree.html).
© The Author(s) 2015. Published by Oxford University Press on behalf of Nucleic Acids Research.

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Year:  2015        PMID: 26578606      PMCID: PMC4770205          DOI: 10.1093/nar/gkv1102

Source DB:  PubMed          Journal:  Nucleic Acids Res        ISSN: 0305-1048            Impact factor:   16.971


  25 in total

1.  PennCNV: an integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data.

Authors:  Kai Wang; Mingyao Li; Dexter Hadley; Rui Liu; Joseph Glessner; Struan F A Grant; Hakon Hakonarson; Maja Bucan
Journal:  Genome Res       Date:  2007-10-05       Impact factor: 9.043

2.  Whole-genome and whole-exome sequencing of bladder cancer identifies frequent alterations in genes involved in sister chromatid cohesion and segregation.

Authors:  Guangwu Guo; Xiaojuan Sun; Chao Chen; Song Wu; Peide Huang; Zesong Li; Michael Dean; Yi Huang; Wenlong Jia; Quan Zhou; Aifa Tang; Zuoquan Yang; Xianxin Li; Pengfei Song; Xiaokun Zhao; Rui Ye; Shiqiang Zhang; Zhao Lin; Mingfu Qi; Shengqing Wan; Liangfu Xie; Fan Fan; Michael L Nickerson; Xiangjun Zou; Xueda Hu; Li Xing; Zhaojie Lv; Hongbin Mei; Shengjie Gao; Chaozhao Liang; Zhibo Gao; Jingxiao Lu; Yuan Yu; Chunxiao Liu; Lin Li; Xiaodong Fang; Zhimao Jiang; Jie Yang; Cailing Li; Xin Zhao; Jing Chen; Fang Zhang; Yongqi Lai; Zheguang Lin; Fangjian Zhou; Hao Chen; Hsiao Chang Chan; Shirley Tsang; Dan Theodorescu; Yingrui Li; Xiuqing Zhang; Jian Wang; Huanming Yang; Yaoting Gui; Jun Wang; Zhiming Cai
Journal:  Nat Genet       Date:  2013-10-13       Impact factor: 38.330

3.  Exome sequencing-based copy-number variation and loss of heterozygosity detection: ExomeCNV.

Authors:  Jarupon Fah Sathirapongsasuti; Hane Lee; Basil A J Horst; Georg Brunner; Alistair J Cochran; Scott Binder; John Quackenbush; Stanley F Nelson
Journal:  Bioinformatics       Date:  2011-08-09       Impact factor: 6.937

Review 4.  An assessment of computational methods for estimating purity and clonality using genomic data derived from heterogeneous tumor tissue samples.

Authors:  Vinod Kumar Yadav; Subhajyoti De
Journal:  Brief Bioinform       Date:  2014-02-20       Impact factor: 11.622

5.  Transgenic oncogenes induce oncogene-independent cancers with individual karyotypes and phenotypes.

Authors:  Andreas Klein; Nan Li; Joshua M Nicholson; Amanda A McCormack; Adolf Graessmann; Peter Duesberg
Journal:  Cancer Genet Cytogenet       Date:  2010-07-15

6.  The life history of 21 breast cancers.

Authors:  Serena Nik-Zainal; Peter Van Loo; David C Wedge; Ludmil B Alexandrov; Christopher D Greenman; King Wai Lau; Keiran Raine; David Jones; John Marshall; Manasa Ramakrishna; Adam Shlien; Susanna L Cooke; Jonathan Hinton; Andrew Menzies; Lucy A Stebbings; Catherine Leroy; Mingming Jia; Richard Rance; Laura J Mudie; Stephen J Gamble; Philip J Stephens; Stuart McLaren; Patrick S Tarpey; Elli Papaemmanuil; Helen R Davies; Ignacio Varela; David J McBride; Graham R Bignell; Kenric Leung; Adam P Butler; Jon W Teague; Sancha Martin; Goran Jönsson; Odette Mariani; Sandrine Boyault; Penelope Miron; Aquila Fatima; Anita Langerød; Samuel A J R Aparicio; Andrew Tutt; Anieta M Sieuwerts; Åke Borg; Gilles Thomas; Anne Vincent Salomon; Andrea L Richardson; Anne-Lise Børresen-Dale; P Andrew Futreal; Michael R Stratton; Peter J Campbell
Journal:  Cell       Date:  2012-05-17       Impact factor: 41.582

7.  AbsCN-seq: a statistical method to estimate tumor purity, ploidy and absolute copy numbers from next-generation sequencing data.

Authors:  Lei Bao; Minya Pu; Karen Messer
Journal:  Bioinformatics       Date:  2014-01-02       Impact factor: 6.937

Review 8.  Clonal and non-clonal chromosome aberrations and genome variation and aberration.

Authors:  Henry H Q Heng; Guo Liu; Steven Bremer; Karen J Ye; Joshua Stevens; Christine J Ye
Journal:  Genome       Date:  2006-03       Impact factor: 2.166

Review 9.  Clonal evolution in cancer.

Authors:  Mel Greaves; Carlo C Maley
Journal:  Nature       Date:  2012-01-18       Impact factor: 49.962

10.  Tumour evolution inferred by single-cell sequencing.

Authors:  Nicholas Navin; Jude Kendall; Jennifer Troge; Peter Andrews; Linda Rodgers; Jeanne McIndoo; Kerry Cook; Asya Stepansky; Dan Levy; Diane Esposito; Lakshmi Muthuswamy; Alex Krasnitz; W Richard McCombie; James Hicks; Michael Wigler
Journal:  Nature       Date:  2011-03-13       Impact factor: 49.962

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  6 in total

Review 1.  Informatics for cancer immunotherapy.

Authors:  J Hammerbacher; A Snyder
Journal:  Ann Oncol       Date:  2017-12-01       Impact factor: 32.976

2.  Identification of Copy Number Alterations from Next-Generation Sequencing Data.

Authors:  Sheida Nabavi; Fatima Zare
Journal:  Adv Exp Med Biol       Date:  2022       Impact factor: 2.622

3.  Comparing single-target and multitarget approaches for postoperative circulating tumour DNA detection in stage II-III colorectal cancer patients.

Authors:  Tenna Vesterman Henriksen; Thomas Reinert; Mads Heilskov Rasmussen; Christina Demuth; Uffe Schou Løve; Anders Husted Madsen; Kåre Andersson Gotschalck; Lene Hjerrild Iversen; Claus Lindbjerg Andersen
Journal:  Mol Oncol       Date:  2022-08-18       Impact factor: 7.449

4.  The subclonal structure and genomic evolution of oral squamous cell carcinoma revealed by ultra-deep sequencing.

Authors:  Siavosh Tabatabaeifar; Mads Thomassen; Martin J Larsen; Stine R Larsen; Torben A Kruse; Jens A Sørensen
Journal:  Oncotarget       Date:  2017-03-07

5.  Genomic Analyses of Breast Cancer Progression Reveal Distinct Routes of Metastasis Emergence.

Authors:  Anne Bruun Krøigård; Martin Jakob Larsen; Charlotte Brasch-Andersen; Anne-Vibeke Lænkholm; Ann S Knoop; Jeanette Dupont Jensen; Martin Bak; Jan Mollenhauer; Mads Thomassen; Torben A Kruse
Journal:  Sci Rep       Date:  2017-03-09       Impact factor: 4.379

6.  Examining the contribution of smoking and HPV towards the etiology of oral cavity squamous cell carcinoma using high-throughput sequencing: A prospective observational study.

Authors:  Andrew P Zammit; Rohit Sinha; Caroline L Cooper; Christopher F L Perry; Ian H Frazer; Zewen K Tuong
Journal:  PLoS One       Date:  2018-10-11       Impact factor: 3.240

  6 in total

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