Literature DB >> 15618527

A method for calling gains and losses in array CGH data.

Pei Wang1, Young Kim, Jonathan Pollack, Balasubramanian Narasimhan, Robert Tibshirani.   

Abstract

Array CGH is a powerful technique for genomic studies of cancer. It enables one to carry out genome-wide screening for regions of genetic alterations, such as chromosome gains and losses, or localized amplifications and deletions. In this paper, we propose a new algorithm 'Cluster along chromosomes' (CLAC) for the analysis of array CGH data. CLAC builds hierarchical clustering-style trees along each chromosome arm (or chromosome), and then selects the 'interesting' clusters by controlling the False Discovery Rate (FDR) at a certain level. In addition, it provides a consensus summary across a set of arrays, as well as an estimate of the corresponding FDR. We illustrate the method using an application of CLAC on a lung cancer microarray CGH data set as well as a BAC array CGH data set of aneuploid cell strains.

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Year:  2005        PMID: 15618527     DOI: 10.1093/biostatistics/kxh017

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


  77 in total

1.  Meiotic chromosome segregation in triploid strains of Saccharomyces cerevisiae.

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Journal:  Genetics       Date:  2010-08-09       Impact factor: 4.562

2.  Deletion at fragile sites is a common and early event in Barrett's esophagus.

Authors:  Lisa A Lai; Rumen Kostadinov; Michael T Barrett; Daniel A Peiffer; Dimitry Pokholok; Robert Odze; Carissa A Sanchez; Carlo C Maley; Brian J Reid; Kevin L Gunderson; Peter S Rabinovitch
Journal:  Mol Cancer Res       Date:  2010-07-20       Impact factor: 5.852

3.  A double-layered mixture model for the joint analysis of DNA copy number and gene expression data.

Authors:  Hyungwon Choi; Zhaohui S Qin; Debashis Ghosh
Journal:  J Comput Biol       Date:  2010-02       Impact factor: 1.479

4.  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

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.  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

7.  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 8.  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

Review 9.  Implications of germline copy-number variations in psychiatric disorders: review of large-scale genetic studies.

Authors:  Masahiro Nakatochi; Itaru Kushima; Norio Ozaki
Journal:  J Hum Genet       Date:  2020-09-21       Impact factor: 3.172

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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