Date of Publication

2021

Document Type

Master's Thesis

Degree Name

Master of Science in Statistics

Subject Categories

Mathematics

College

College of Science

Department/Unit

Mathematics and Statistics Department

Thesis Advisor

Frumencio F. Co

Defense Panel Chair

Rechel G. Arcilla

Defense Panel Member

Romeric F. Pobre
Erold Ryan A. Bonzo

Abstract/Summary

Digital PCR (dPCR) is an emerging technology to detect and quantify target DNA sequences for applications such as medical diagnosis, forensic research, and food safety analysis. As the use of dPCR gains more popularity in recent years, each step in its workflow must be improved to surpass its performance over the gold standard real-time qPCR. Its novel approach in partitioning target samples into equal-sized droplets makes it appealing to be more theoretically accurate than qPCR. Droplets containing at least one target DNA emits a high fluorescence intensity and is classified as positive; otherwise, low intensity is emitted and is classified as negative. Classification becomes complicated when several intermediate droplets called "rain" are present, causing severe misclassification. Since nonoptimal data is frequent in dPCR studies, droplet classifiers should be robust to the presence of rain, baseline shifts, multiple fluorescence populations, and poor separation of populations. This thesis reviews the current droplet classification methods of single-channel dPCR quantification, which are Cloudy, ddpcRquant, and Umbrella. The Expectation-Maximization (EM) Clustering is proposed to address plausible research gaps and improve current classification performance in the dataset with samples of varying quality from Lievens et al. (2017) and a simulated dataset. The results show that the proposed method using T- and skewed T-mixture models have mostly outperformed the precision in terms of CV amongst three current methods, and is on par or better in terms of accuracy and linearity of target concentration estimates. Finally, the proposed method is freely available for public use by installing the “popPCR” R package from CRAN (The Comprehensive R Archive Network).

Abstract Format

html

Language

English

Format

Electronic

Physical Description

109 leaves

Keywords

Polymerase chain reaction; Technology; Drops

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Embargo Period

5-5-2021

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