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A probe-density-based analysis method for array CGH data: simulation, normalization and centralization.


ABSTRACT: Genomic instability is one of the fundamental factors in tumorigenesis and tumor progression. Many studies have shown that copy-number abnormalities at the DNA level are important in the pathogenesis of cancer. Array comparative genomic hybridization (aCGH), developed based on expression microarray technology, can reveal the chromosomal aberrations in segmental copies at a high resolution. However, due to the nature of aCGH, many standard expression data processing tools, such as data normalization, often fail to yield satisfactory results.We demonstrated a novel aCGH normalization algorithm, which provides an accurate aCGH data normalization by utilizing the dependency of neighboring probe measurements in aCGH experiments. To facilitate the study, we have developed a hidden Markov model (HMM) to simulate a series of aCGH experiments with random DNA copy number alterations that are used to validate the performance of our normalization. In addition, we applied the proposed normalization algorithm to an aCGH study of lung cancer cell lines. By using the proposed algorithm, data quality and the reliability of experimental results are significantly improved, and the distinct patterns of DNA copy number alternations are observed among those lung cancer cell lines.Source codes and.gures may be found at http://ntumaps.cgm.ntu.edu.tw/aCGH_supplementary.

SUBMITTER: Chen HI 

PROVIDER: S-EPMC2732214 | biostudies-literature | 2008 Aug

REPOSITORIES: biostudies-literature

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A probe-density-based analysis method for array CGH data: simulation, normalization and centralization.

Chen Hung-I Harry HI   Hsu Fang-Han FH   Jiang Yuan Y   Tsai Mong-Hsun MH   Yang Pan-Chyr PC   Meltzer Paul S PS   Chuang Eric Y EY   Chen Yidong Y  

Bioinformatics (Oxford, England) 20080704 16


<h4>Motivation</h4>Genomic instability is one of the fundamental factors in tumorigenesis and tumor progression. Many studies have shown that copy-number abnormalities at the DNA level are important in the pathogenesis of cancer. Array comparative genomic hybridization (aCGH), developed based on expression microarray technology, can reveal the chromosomal aberrations in segmental copies at a high resolution. However, due to the nature of aCGH, many standard expression data processing tools, such  ...[more]

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