This collection includes both ASU Theses and Dissertations, submitted by graduate students, and the Barrett, Honors College theses submitted by undergraduate students. 

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Description
Peptide microarrays have been used in molecular biology to profile immune responses and develop diagnostic tools. When the microarrays are printed with random peptide sequences, they can be used to identify antigen antibody binding patterns or immunosignatures. In this thesis, an advanced signal processing method is proposed to estimate

Peptide microarrays have been used in molecular biology to profile immune responses and develop diagnostic tools. When the microarrays are printed with random peptide sequences, they can be used to identify antigen antibody binding patterns or immunosignatures. In this thesis, an advanced signal processing method is proposed to estimate epitope antigen subsequences as well as identify mimotope antigen subsequences that mimic the structure of epitopes from random-sequence peptide microarrays. The method first maps peptide sequences to linear expansions of highly-localized one-dimensional (1-D) time-varying signals and uses a time-frequency processing technique to detect recurring patterns in subsequences. This technique is matched to the aforementioned mapping scheme, and it allows for an inherent analysis on how substitutions in the subsequences can affect antibody binding strength. The performance of the proposed method is demonstrated by estimating epitopes and identifying potential mimotopes for eight monoclonal antibody samples.

The proposed mapping is generalized to express information on a protein's sequence location, structure and function onto a highly localized three-dimensional (3-D) Gaussian waveform. In particular, as analysis of protein homology has shown that incorporating different kinds of information into an alignment process can yield more robust alignment results, a pairwise protein structure alignment method is proposed based on a joint similarity measure of multiple mapped protein attributes. The 3-D mapping allocates protein properties into distinct regions in the time-frequency plane in order to simplify the alignment process by including all relevant information into a single, highly customizable waveform. Simulations demonstrate the improved performance of the joint alignment approach to infer relationships between proteins, and they provide information on mutations that cause changes to both the sequence and structure of a protein.

In addition to the biology-based signal processing methods, a statistical method is considered that uses a physics-based model to improve processing performance. In particular, an externally developed physics-based model for sea clutter is examined when detecting a low radar cross-section target in heavy sea clutter. This novel model includes a process that generates random dynamic sea clutter based on the governing physics of water gravity and capillary waves and a finite-difference time-domain electromagnetics simulation process based on Maxwell's equations propagating the radar signal. A subspace clutter suppression detector is applied to remove dominant clutter eigenmodes, and its improved performance over matched filtering is demonstrated using simulations.
ContributorsO'Donnell, Brian (Author) / Papandreou-Suppappola, Antonia (Thesis advisor) / Bliss, Daniel (Committee member) / Johnston, Stephen A. (Committee member) / Kovvali, Narayan (Committee member) / Tepedelenlioğlu, Cihan (Committee member) / Arizona State University (Publisher)
Created2014
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Description
The continuous time-tagging of photon arrival times for high count rate sources isnecessary for applications such as optical communications, quantum key encryption, and astronomical measurements. Detection of Hanbury-Brown and Twiss (HBT) single photon correlations from thermal sources, such as stars, requires a combination of high dynamic range, long integration times, and low systematics

The continuous time-tagging of photon arrival times for high count rate sources isnecessary for applications such as optical communications, quantum key encryption, and astronomical measurements. Detection of Hanbury-Brown and Twiss (HBT) single photon correlations from thermal sources, such as stars, requires a combination of high dynamic range, long integration times, and low systematics in the photon detection and time tagging system. The continuous nature of the measurements and the need for highly accurate timing resolution requires a customized time-to-digital converter (TDC). A custom built, two-channel, field programmable gate array (FPGA)-based TDC capable of continuously time tagging single photons with sub clock cycle timing resolution was characterized. Auto-correlation and cross-correlation measurements were used to constrain spurious systematic effects in the pulse count data as a function of system variables. These variables included, but were not limited to, incident photon count rate, incoming signal attenuation, and measurements of fixed signals. Additionally, a generalized likelihood ratio test using maximum likelihood estimators (MLEs) was derived as a means to detect and estimate correlated photon signal parameters. The derived GLRT was capable of detecting correlated photon signals in a laboratory setting with a high degree of statistical confidence. A proof is presented in which the MLE for the amplitude of the correlated photon signal is shown to be the minimum variance unbiased estimator (MVUE). The fully characterized TDC was used in preliminary measurements of astronomical sources using ground based telescopes. Finally, preliminary theoretical groundwork is established for the deep space optical communications system of the proposed Breakthrough Starshot project, in which low-mass craft will travel to the Alpha Centauri system to collect scientific data from Proxima B. This theoretical groundwork utilizes recent and upcoming space based optical communication systems as starting points for the Starshot communication system.
ContributorsHodges, Todd Michael William (Author) / Mauskopf, Philip (Thesis advisor) / Trichopoulos, George (Thesis advisor) / Papandreou-Suppappola, Antonia (Committee member) / Bliss, Daniel (Committee member) / Arizona State University (Publisher)
Created2022