Literature DB >> 17855472

Stochastic segmentation models for array-based comparative genomic hybridization data analysis.

Tze Leung Lai1, Haipeng Xing, Nancy Zhang.   

Abstract

Array-based comparative genomic hybridization (array-CGH) is a high throughput, high resolution technique for studying the genetics of cancer. Analysis of array-CGH data typically involves estimation of the underlying chromosome copy numbers from the log fluorescence ratios and segmenting the chromosome into regions with the same copy number at each location. We propose for the analysis of array-CGH data, a new stochastic segmentation model and an associated estimation procedure that has attractive statistical and computational properties. An important benefit of this Bayesian segmentation model is that it yields explicit formulas for posterior means, which can be used to estimate the signal directly without performing segmentation. Other quantities relating to the posterior distribution that are useful for providing confidence assessments of any given segmentation can also be estimated by using our method. We propose an approximation method whose computation time is linear in sequence length which makes our method practically applicable to the new higher density arrays. Simulation studies and applications to real array-CGH data illustrate the advantages of the proposed approach.

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Year:  2007        PMID: 17855472     DOI: 10.1093/biostatistics/kxm031

Source DB:  PubMed          Journal:  Biostatistics        ISSN: 1465-4644            Impact factor:   5.899


  19 in total

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Authors:  Gen Nowak; Trevor Hastie; Jonathan R Pollack; Robert Tibshirani
Journal:  Biostatistics       Date:  2011-06-03       Impact factor: 5.899

2.  Parent-specific copy number in paired tumor-normal studies using circular binary segmentation.

Authors:  Adam B Olshen; Henrik Bengtsson; Pierre Neuvial; Paul T Spellman; Richard A Olshen; Venkatraman E Seshan
Journal:  Bioinformatics       Date:  2011-06-11       Impact factor: 6.937

3.  Detecting simultaneous changepoints in multiple sequences.

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Journal:  Biometrika       Date:  2010-06-16       Impact factor: 2.445

4.  Multiple Change-Point Detection via a Screening and Ranking Algorithm.

Authors:  Ning Hao; Yue Selena Niu; Heping Zhang
Journal:  Stat Sin       Date:  2013-07-01       Impact factor: 1.261

5.  A Semiparametric Change-Point Regression Model for Longitudinal Observations.

Authors:  Haipeng Xing; Zhiliang Ying
Journal:  J Am Stat Assoc       Date:  2012-12-01       Impact factor: 5.033

6.  Sequential model selection-based segmentation to detect DNA copy number variation.

Authors:  Jianhua Hu; Liwen Zhang; Huixia Judy Wang
Journal:  Biometrics       Date:  2016-03-08       Impact factor: 2.571

7.  A classification model for distinguishing copy number variants from cancer-related alterations.

Authors:  Irina Ostrovnaya; Gouri Nanjangud; Adam B Olshen
Journal:  BMC Bioinformatics       Date:  2010-06-02       Impact factor: 3.169

8.  Genome-wide association study of multiplex schizophrenia pedigrees.

Authors:  Douglas F Levinson; Jianxin Shi; Kai Wang; Sang Oh; Brien Riley; Ann E Pulver; Dieter B Wildenauer; Claudine Laurent; Bryan J Mowry; Pablo V Gejman; Michael J Owen; Kenneth S Kendler; Gerald Nestadt; Sibylle G Schwab; Jacques Mallet; Deborah Nertney; Alan R Sanders; Nigel M Williams; Brandon Wormley; Virginia K Lasseter; Margot Albus; Stephanie Godard-Bauché; Madeline Alexander; Jubao Duan; Michael C O'Donovan; Dermot Walsh; Anthony O'Neill; George N Papadimitriou; Dimitris Dikeos; Wolfgang Maier; Bernard Lerer; Dominique Campion; David Cohen; Maurice Jay; Ayman Fanous; Peter Eichhammer; Jeremy M Silverman; Nadine Norton; Nancy Zhang; Hakon Hakonarson; Cynthia Gao; Ami Citri; Mark Hansen; Stephan Ripke; Frank Dudbridge; Peter A Holmans
Journal:  Am J Psychiatry       Date:  2012-09       Impact factor: 18.112

9.  Segmentation and estimation for SNP microarrays: a Bayesian multiple change-point approach.

Authors:  Yu Chuan Tai; Mark N Kvale; John S Witte
Journal:  Biometrics       Date:  2010-09       Impact factor: 2.571

10.  A statistical change point model approach for the detection of DNA copy number variations in array CGH data.

Authors:  Jie Chen; Yu-Ping Wang
Journal:  IEEE/ACM Trans Comput Biol Bioinform       Date:  2009 Oct-Dec       Impact factor: 3.710

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