Authors

Andrea Roberson

Type

Text

Type

Dissertation

Advisor

Finch, Stephen J. | Nancy R. Mendell | Wei Zhu | Derek Gordon.

Date

2010-05-01

Keywords

Bayesian, CNV, Comparison, Hidden, Markov, Models | Applied Mathematics -- Statistics

Department

Department of Applied Mathematics and Statistics

Language

en_US

Source

This work is sponsored by the Stony Brook University Graduate School in compliance with the requirements for completion of degree.

Identifier

http://hdl.handle.net/11401/72652

Publisher

The Graduate School, Stony Brook University: Stony Brook, NY.

Format

application/pdf

Abstract

Array comparative genomic hybridization (aCGH) can detect copy number variation (CNV) across the genome. Five current Hidden Markov Model (HMM) software systems for estimating copy number variation with aCGH data were compared. These comparisons were in terms of their effectiveness for identifying CNVs in simulated data based on the ratio of signal intensities. There was significant variability in the error rates. The system that adjusted for outliers in the model, the Robust Hidden Markov Model (HMM-R), appeared to have the best performance. The emission density function of the HMM is a mixture of two normal densities, in which one component represents usable aCGH data and the other represents outliers. HMM-R correctly classified 99.8% of normal states, 84.5% of CNV gains, and 90.2% of CNV losses. That is, error rates with regard to gains and losses were appreciable even with the best software. The HMM-R method demonstrated higher sensitivity and lower false discovery rates than the commonly used procedure. While the accuracy rates of HMM software has improved, there is substantial room for further improvement.

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