Literature DB >> 15572474

Quantile smoothing of array CGH data.

Paul H C Eilers1, Renée X de Menezes.   

Abstract

MOTIVATION: Plots of array Comparative Genomic Hybridization (CGH) data often show special patterns: stretches of constant level (copy number) with sharp jumps between them. There can also be much noise. Classic smoothing algorithms do not work well, because they introduce too much rounding. To remedy this, we introduce a fast and effective smoothing algorithm based on penalized quantile regression. It can compute arbitrary quantile curves, but we concentrate on the median to show the trend and the lower and upper quartile curves showing the spread of the data. Two-fold cross-validation is used for optimizing the weight of the penalties.
RESULTS: Simulated data and a published dataset are used to show the capabilities of the method to detect the segments of changed copy numbers in array CGH data.

Mesh:

Year:  2004        PMID: 15572474     DOI: 10.1093/bioinformatics/bti148

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


  52 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.  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

4.  Efficient inference of local ancestry.

Authors:  James J Yang; Jia Li; Anne Buu; L K Williams
Journal:  Bioinformatics       Date:  2013-08-19       Impact factor: 6.937

5.  Bayesian Frequentist hybrid Model wth Application to the Analysis of Gene Copy Number Changes.

Authors:  Ao Yuan; Guanjie Chen; Juan Xiong; Wenqing He; Charles Rotimi
Journal:  J Appl Stat       Date:  2011       Impact factor: 1.404

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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