Literature DB >> 15772101

Denoising array-based comparative genomic hybridization data using wavelets.

Li Hsu1, Steven G Self, Douglas Grove, Tim Randolph, Kai Wang, Jeffrey J Delrow, Lenora Loo, Peggy Porter.   

Abstract

Array-based comparative genomic hybridization (array-CGH) provides a high-throughput, high-resolution method to measure relative changes in DNA copy number simultaneously at thousands of genomic loci. Typically, these measurements are reported and displayed linearly on chromosome maps, and gains and losses are detected as deviations from normal diploid cells. We propose that one may consider denoising the data to uncover the true copy number changes before drawing inferences on the patterns of aberrations in the samples. Nonparametric techniques are particularly suitable for data denoising as they do not impose a parametric model in finding structures in the data. In this paper, we employ wavelets to denoise the data as wavelets have sound theoretical properties and a fast computational algorithm, and are particularly well suited for handling the abrupt changes seen in array-CGH data. A simulation study shows that denoising data prior to testing can achieve greater power in detecting the aberrant spot than using the raw data without denoising. Finally, we illustrate the method on two array-CGH data sets.

Mesh:

Substances:

Year:  2005        PMID: 15772101     DOI: 10.1093/biostatistics/kxi004

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


  66 in total

1.  Bayesian Random Segmentation Models to Identify Shared Copy Number Aberrations for Array CGH Data.

Authors:  Veerabhadran Baladandayuthapani; Yuan Ji; Rajesh Talluri; Luis E Nieto-Barajas; Jeffrey S Morris
Journal:  J Am Stat Assoc       Date:  2010-12       Impact factor: 5.033

2.  Comparative analysis of algorithms for identifying amplifications and deletions in array CGH data.

Authors:  Weil R Lai; Mark D Johnson; Raju Kucherlapati; Peter J Park
Journal:  Bioinformatics       Date:  2005-08-04       Impact factor: 6.937

3.  A novel signal processing approach for the detection of copy number variations in the human genome.

Authors:  Catherine Stamoulis; Rebecca A Betensky
Journal:  Bioinformatics       Date:  2011-07-12       Impact factor: 6.937

4.  Sparse representation and Bayesian detection of genome copy number alterations from microarray data.

Authors:  Roger Pique-Regi; Jordi Monso-Varona; Antonio Ortega; Robert C Seeger; Timothy J Triche; Shahab Asgharzadeh
Journal:  Bioinformatics       Date:  2008-01-18       Impact factor: 6.937

5.  MSB: a mean-shift-based approach for the analysis of structural variation in the genome.

Authors:  Lu-Yong Wang; Alexej Abyzov; Jan O Korbel; Michael Snyder; Mark Gerstein
Journal:  Genome Res       Date:  2008-11-26       Impact factor: 9.043

6.  Hidden Markov models for the assessment of chromosomal alterations using high-throughput SNP arrays.

Authors:  Robert B Scharpf; Giovanni Parmigiani; Jonathan Pevsner; Ingo Ruczinski
Journal:  Ann Appl Stat       Date:  2008-06-01       Impact factor: 2.083

Review 7.  Statistical issues in the analysis of DNA Copy Number Variations.

Authors:  Nathan E Wineinger; Richard E Kennedy; Stephen W Erickson; Mary K Wojczynski; Carl E Bruder; Hemant K Tiwari
Journal:  Int J Comput Biol Drug Des       Date:  2008

8.  Novel multisample scheme for inferring phylogenetic markers from whole genome tumor profiles.

Authors:  Ayshwarya Subramanian; Stanley Shackney; Russell Schwartz
Journal:  IEEE/ACM Trans Comput Biol Bioinform       Date:  2013 Nov-Dec       Impact factor: 3.710

9.  A fused lasso latent feature model for analyzing multi-sample aCGH data.

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

10.  An improved method for detecting and delineating genomic regions with altered gene expression in cancer.

Authors:  Björn Nilsson; Mikael Johansson; Anders Heyden; Sven Nelander; Thoas Fioretos
Journal:  Genome Biol       Date:  2008-01-21       Impact factor: 13.583

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