UMD Theses and Dissertations

Permanent URI for this collectionhttp://hdl.handle.net/1903/3

New submissions to the thesis/dissertation collections are added automatically as they are received from the Graduate School. Currently, the Graduate School deposits all theses and dissertations from a given semester after the official graduation date. This means that there may be up to a 4 month delay in the appearance of a given thesis/dissertation in DRUM.

More information is available at Theses and Dissertations at University of Maryland Libraries.

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    Making Predictions and Handling Errors in Reconstructed Biological Networks
    (2013) Platig, John; Girvan, Michelle; Physics; Digital Repository at the University of Maryland; University of Maryland (College Park, Md.)
    In this thesis we present methods for applying techniques from complex network theory to analyze and interpret inferred biological interactions. With the advent of high throughput technologies such as gene microarrays and genome-wide sequencing, it is now possible to measure the activity of every gene in a cancer cell population under different conditions. How to extract important interactions from these experiments remains an outstanding question. Here we present a method to identify these key interactions by focusing on short paths in a transcription factor network. We use a mutual information-based approach to infer the transcription factor network from gene expression microarrays, which measure perturbations in a Diffuse Large B Cell Lymphoma cell line. By focusing on the number of short paths between transcription factors and signature genes in the inferred network, we find a set of transcription factors whose biology is crucial to the continued survival of these lymphoma cells and also show that a subset of these factors have a distinct expression pattern in patient tumors as well. As many networks of interest are reconstructed from data containing errors, we introduce two simple models of false and missing links to characterize the effects of network misinformation on three commonly used centrality measures: degree centrality, betweenness centrality, and dynamical importance. We show that all three measures are especially robust to both false and missing links when the network has a power law in the tail of its degree distribution.
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    A Systems Engineering Framework for Metabolic Engineering Experiments
    (2011) Johnnie, Joseph George; Austin, Mark; Systems Engineering; Digital Repository at the University of Maryland; University of Maryland (College Park, Md.)
    Cells of living organisms simultaneously operate hundreds or thousands of interconnected chemical reactions. Metabolic networks include these chemical reactions and compounds participating in them. Metabolic engineering is a science centered on the analysis and purposeful modification of an organism's metabolic network toward a beneficial purpose, such as production of fuel or medicinal compounds in microorganisms. Unfortunately, there are problems with the design and visualization of modified metabolic networks due to lack of standardized and fully developed visual modeling languages. The purposes of this paper are to propose a multilevel framework for the synthesis, analysis and design of metabolic systems, and then explore the extent to which abstractions from systems engineering (e.g., SysML) can complement and add value to the abstractions currently under development within the greater biological community (e.g., SBGN). The computational test-bed that accompanies this work is production of the anti-malarial drug artemisinin in genetically engineered Saccaharomyces cerevisiae (yeast).