Literature DB >> 12837263

Array rank order regression analysis for the detection of gene copy-number changes in human cancer.

Chun Cheng1, Robert Kimmel, Paul Neiman, Lue Ping Zhao.   

Abstract

cDNA microarray technology has been applied to the detection of DNA copy-number changes in malignant tumors. Test and control genomic DNA samples are differentially labeled and cohybridized to a spotted cDNA microarray. The ratio of test to control fluorescence intensities for each spot reflects relative gene copy number. The low signal-to-noise ratios of this assay and the variable levels of gene amplification and deletion among tumors hamper the detection of deviations from the diploid complement. We describe a regression-based statistical method to test for altered copy number on each gene and apply the technique to copy-number profiles in 10 thyroid tumors. We show that a novel transformation of fluorescence ratios into array rank order efficiently normalizes the heterogeneity among copy-number profiles and improves the reproducibility of the results. Array rank order regression analysis enhances the detection of consistent changes in gene copy number in solid tumors by cDNA microarray-based comparative genome hybridization.

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Year:  2003        PMID: 12837263     DOI: 10.1016/s0888-7543(03)00122-8

Source DB:  PubMed          Journal:  Genomics        ISSN: 0888-7543            Impact factor:   5.736


  6 in total

1.  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

2.  Bayesian Hidden Markov Modeling of Array CGH Data.

Authors:  Subharup Guha; Yi Li; Donna Neuberg
Journal:  J Am Stat Assoc       Date:  2008-06-01       Impact factor: 5.033

3.  Detecting genomic aberrations using products in a multiscale analysis.

Authors:  Xuesong Yu; Timothy W Randolph; Hua Tang; Li Hsu
Journal:  Biometrics       Date:  2010-09       Impact factor: 2.571

Review 4.  A survey of analysis software for array-comparative genomic hybridisation studies to detect copy number variation.

Authors:  Anis Karimpour-Fard; Laura Dumas; Tzulip Phang; James M Sikela; Lawrence E Hunter
Journal:  Hum Genomics       Date:  2010-08       Impact factor: 4.639

5.  A systematic search for SNPs/haplotypes associated with disease phenotypes using a haplotype-based stepwise procedure.

Authors:  Yin Yang; Shuying Sue Li; Jason W Chien; Jessica Andriesen; Lue Ping Zhao
Journal:  BMC Genet       Date:  2008-12-22       Impact factor: 2.797

6.  Gene copy number analysis for family data using semiparametric copula model.

Authors:  Ao Yuan; Guanjie Chen; Zhong-Cheng Zhou; George Bonney; Charles Rotimi
Journal:  Bioinform Biol Insights       Date:  2008-09-26
  6 in total

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