Monitoring and Control Framework for Advanced Power Plant Systems Using Artificial Intelligence Techniques

This dissertation presents the design, development, and simulation testing of a monitoring and control framework for dynamic systems using artificial intelligence techniques. A comprehensive monitoring and control system capable of detecting, identifying, evaluating, and accommodating various subsystem failures and upset conditions is presented. The system is developed by synergistically merging concepts inspired from the biological immune system with evolutionary optimization algorithms and adaptive control techniques.;The proposed methodology provides the tools for addressing the complexity and multi-dimensionality of the modern power plants in a comprehensive and integrated manner that classical approaches cannot achieve. Current approaches typically address abnormal condition (AC) detection of isolated subsystems of low complexity, affected by specific AC involving few features with limited identification capability. They do not attempt AC evaluation and mostly rely on control system robustness for accommodation. Addressing the problem of power plant monitoring and control under AC at this level of completeness has not yet been attempted.;Within the proposed framework, a novel algorithm, namely the partition of the universe, was developed for building the artificial immune system self. As compared to the clustering approach, the proposed approach is less computationally intensive and facilitates the use of full-dimensional self for system AC detection, identification, and evaluation. The approach is implemented in conjunction with a modified and improved dendritic cell algorithm. It allows for identifying the failed subsystems without previous training and is extended to address the AC evaluation using a novel approach.;The adaptive control laws are designed to augment the performance and robustness of baseline control laws under normal and abnormal operating conditions. Artificial neural network-based and artificial immune system-based approaches are developed and investigated for an advanced power plant through numerical simulation.;This dissertation also presents the development of an interactive computational environment for the optimization of power plant control system using evolutionary techniques with immunity-inspired enhancements. Several algorithms mimicking mechanisms of the immune system of superior organisms, such as cloning, affinity-based selection, seeding, and vaccination are used. These algorithms are expected to enhance the computational effectiveness, improve convergence, and be more efficient in handling multiple local extrema, through an adequate balance between exploration and exploitation.;The monitoring and control framework formulated in this dissertation applies to a wide range of technical problems. The proposed methodology is demonstrated with promising results using a high validity DynsimRTM model of the acid gas removal unit that is part of the integrated gasification combined cycle power plant available at West Virginia University AVESTAR Center. The obtained results show that the proposed system is an efficient and valuable technique to be applied to a real world application. The implementation of this methodology can potentially have significant impacts on the operational safety of many complex systems

A SOM+ Diagnostic System for Network Intrusion Detection

This research created a new theoretical Soft Computing (SC) hybridized network intrusion detection diagnostic system including complex hybridization of a 3D full color Self-Organizing Map (SOM), Artificial Immune System Danger Theory (AISDT), and a Fuzzy Inference System (FIS). This SOM+ diagnostic archetype includes newly defined intrusion types to facilitate diagnostic analysis, a descriptive computational model, and an Invisible Mobile Network Bridge (IMNB) to collect data, while maintaining compatibility with traditional packet analysis. This system is modular, multitaskable, scalable, intuitive, adaptable to quickly changing scenarios, and uses relatively few resources

Integrated Immunity-based Methodology for UAV Monitoring and Control

A general integrated and comprehensive health management framework based on the artificial immune system (AIS) paradigm is formulated and an automated system is developed and tested through simulation for the detection, identification, evaluation, and accommodation (DIEA) of abnormal conditions (ACs) on an unmanned aerial vehicle (UAV). The proposed methodology involves the establishment of a body of data to represent the function of the vehicle under nominal conditions, called the self, and differentiating this operation from that of the vehicle under an abnormal condition, referred to as the non-self. Data collected from simulations of the selected UAV autonomously flying a set of prescribed trajectories were used to develop and test novel schemes that are capable of addressing the AC-DIEA of sensor and actuator faults on a UAV. While the specific dynamic system used here is a UAV, the proposed framework and methodology is general enough to be adapted and applied to any complex dynamic system. The ACs considered within this effort included aerodynamic control surface locks and damage and angular rate sensor biases. The general framework for the comprehensive health management system comprises a novel complete integration of the AC-DIEA process with focus on the transition between the four different phases. The hierarchical multiself (HMS) strategy is used in conjunction with several biomimetic mechanisms to address the various steps in each phase. The partition of the universe approach is used as the basis of the AIS generation and the binary detection phase. The HMS approach is augmented by a mechanism inspired by the antigen presenting cells of the adaptive immune system for performing AC identification. The evaluation and accommodation phases are the most challenging phases of the AC-DIEA process due to the complexity and diversity of the ACs and the multidimensionality of the AIS. Therefore, the evaluation phase is divided into three separate steps: the qualitative evaluation, direct quantitative evaluation, and the indirect quantitative evaluation, where the type, severity, and effects of the AC are determined, respectively. The integration of the accommodation phase is based on a modular process, namely the strategic decision making, tactical decision marking, and execution modules. These modules are designed by the testing of several approaches for integrating the accommodation phase, which are specialized based on the type of AC being addressed. These approaches include redefining of the mission, adjustment or shifting of the control laws, or adjusting the sensor outputs. Adjustments of the mission include redefining of the trajectory to remove maneuvers which are no longer possible, while adjusting of the control laws includes modifying gains involved in determination of commanded control surface deflections. Analysis of the transition between phases includes a discussion of results for integrated example cases where the proposed AC-DIEA process is applied. The cases considered show the validity of the integrated AC-DIEA system and specific accommodation approaches by an improvement in flight performance through metrics that capture trajectory tracking errors and control activity differences between nominal, abnormal, and accommodated cases

Development of On-Tissue Mass Spectrometric Strategies for Protein Identification, Quantification and Mapping

Résumé : L’imagerie par spectrométrie de masse est une technique sans marquage permettant la détection et la localisation de protéines à partir de coupes de tissus. Afin de répondre à des problématiques biologiques, le nombre de protéines identifiées doit être amélioré. Une stratégie consiste à réaliser une micro-jonction liquide sur des régions particulières des coupes de tissus afin d’extraire les peptides issus de la digestion in situ des protéines. Plus de 1500 protéines ont identifié sur une zone de 650µm, correspondant à environ 1900 cellules. Une corrélation entre ces données avec celles générées par MSI a augmenté le nombre de protéines localisées. Afin d’obtenir dans le même temps, la localisation et l’identification de protéines, une méthode consiste à réaliser la microdissection de l’ensemble de la coupe après l’avoir déposée sur une lame recouverte de prafilm. Parafilm-Assisted Microdissection (PAM) a également été appliquée à l’étude de l'expression différentielle de protéines dans des tumeurs de prostate. Les résultats identifiés glutamate oxaloacétate transférase 2 (GOT2) en tant que biomarqueur de protéine candidate impliquée dans le métabolisme du glucose, en plus de celles qui ont déjà été indiqué précédemment. Réunis ensemble, ces méthodes MS d'analyses directes fournissent un moyen robuste d’étude de protéines dans leur état natif afin de fournir des indications sur leur rôle dans des systèmes biologiques. // Abstract : Mass spectrometry-based methods for direct tissue analysis, such as MS imaging, are label-free techniques that permit the detection and localization of proteins on tissue sections. There is a need to improve the number of protein identifications in these techniques for them to comprehensively address biological questions. One strategy to obtain high protein IDs is to realize liquid microjunction on localized regions of tissue sections to extract peptides from the in situ digestion of proteins. More than 1500 proteins were identified in a 650μm spot, corresponding to about 1900 cells. Matching these IDs with those from MSI increased the number of localized proteins. In order to achieve simultaneous identification and localization of proteins, a method consisting of microdissecting entire tissue sections mounted on parafilmcovered slides was developed. Spectral counting was then used to quantify identified proteins, and the values were used to generate images. Parafilm-Assisted Microdissection (PAM) was also used to examine the differential expression of proteins on prostate tumors. Results identified glutamate oxaloacetate transferase 2 (GOT2) as a candidate protein biomarker involved in glucose metabolism, in addition to those that have already been reported previously. Taken together, these direct MS analysis methods provide a robust means of analyzing proteins in their native state and are expected to provide insights to their role in biological systems

Cyber Security and Critical Infrastructures 2nd Volume

The second volume of the book contains the manuscripts that were accepted for publication in the MDPI Special Topic "Cyber Security and Critical Infrastructure" after a rigorous peer-review process. Authors from academia, government and industry contributed their innovative solutions, consistent with the interdisciplinary nature of cybersecurity. The book contains 16 articles, including an editorial that explains the current challenges, innovative solutions and real-world experiences that include critical infrastructure and 15 original papers that present state-of-the-art innovative solutions to attacks on critical systems

Developing a bioinformatics framework for proteogenomics

In the last 15 years, since the human genome was first sequenced, genome sequencing and annotation have continued to improve. However, genome annotation has not kept up with the accelerating rate of genome sequencing and as a result there is now a large backlog of genomic data waiting to be interpreted both quickly and accurately. Through advances in proteomics a new field has emerged to help improve genome annotation, termed proteogenomics, which uses peptide mass spectrometry data, enabling the discovery of novel protein coding genes, as well as the refinement and validation of known and putative protein-coding genes. The annotation of genomes relies heavily on ab initio gene prediction programs and/or mapping of a range of RNA transcripts. Although this method provides insights into the gene content of genomes it is unable to distinguish protein-coding genes from putative non-coding RNA genes. This problem is further confounded by the fact that only 5% of the public protein sequence repository at UniProt/SwissProt has been curated and derived from actual protein evidence. This thesis contends that it is critically important to incorporate proteomics data into genome annotation pipelines to provide experimental protein-coding evidence. Although there have been major improvements in proteogenomics over the last decade there are still numerous challenges to overcome. These key challenges include the loss of sensitivity when using inflated search spaces of putative sequences, how best to interpret novel identifications and how best to control for false discoveries. This thesis addresses the existing gap between the use of genomic and proteomic sources for accurate genome annotation by applying a proteogenomics approach with a customised methodology. This new approach was applied within four case studies: a prokaryote bacterium; a monocotyledonous wheat plant; a dicotyledonous grape plant; and human. The key contributions of this thesis are: a new methodology for proteogenomics analysis; 145 suggested gene refinements in Bradyrhizobium diazoefficiens (nitrogen-fixing bacteria); 55 new gene predictions (57 protein isoforms) in Vitis vinifera (grape); 49 new gene predictions (52 protein isoforms) in Homo sapiens (human); and 67 new gene predictions (70 protein isoforms) in Triticum aestivum (bread wheat). Lastly, a number of possible improvements for the studies conducted in this thesis and proteogenomics as a whole have been identified and discussed

Characterization, classification and alignment of protein-protein interfaces

Protein structural models provide essential information for the research on protein-protein interactions. In this dissertation, we describe two projects on the analysis of protein interactions using structural information. The focus of the first is to characterize and classify different types of interactions. We discriminate between biological obligate and biological non-obligate interactions, and crystal packing contacts. To this end, we defined six interface properties and used them to compare the three types of interactions in a hand-curated dataset. Based on the analysis, a classifier, named NOXclass, was constructed using a support vector machine algorithm in order to generate predictions of interaction types. NOXclass was tested on a non-redundant dataset of 243 protein-protein interactions and reaches an accuracy of 91.8%. The program is benecial for structural biologists for the interpretation of protein quaternary structures and to form hypotheses about the nature of proteinprotein interactions when experimental data are yet unavailable. In the second part of the dissertation, we present Galinter, a novel program for the geometrical comparison of protein-protein interfaces. The Galinter program aims at identifying similar patterns of different non-covalent interactions at interfaces. It is a graph-based approach optimized for aligning non-covalent interactions. A scoring scheme was developed for estimating the statistical signicance of the alignments. We tested the Galinter method on a published dataset of interfaces. Galinter alignments agree with those delivered by methods based on interface residue comparison and backbone structure comparison. In addition, we applied Galinter on four medically relevant examples of protein mimicry. Our results are consistent with previous human-curated analysis. The Galinter program provides an intuitive method of comparative analysis and visualization of binding modes and may assist in the prediction of interaction partners, and the design and engineering of protein interactions and interaction inhibitors

Nanogenomics and Nanoproteomics Enabling Personalized, Predictive and Preventive Medicine

Since the discovery of the nucleic acid, molecular biology has made tremendous progresses, achieving a lot of results. Despite this, there is still a gap between the classical and traditional medical approach and the molecular world. Inspired by the incredible wealth of data generated by the "omics"-driven techniques and the “high-trouhgput technologies” (HTTs), I have tried to develop a protocol that could reduce the actually extant barrier between the phenomenological medicine and the molecular medicine, facilitating a translational shift from the lab to the patient bedside. I also felt the urgent need to integrate the most important omics sciences, that is to say genomics and proteomics. Nucleic Acid Programmable Protein Arrays (NAPPA) can do this, by utilizing a complex mammalian cell free expression system to produce proteins in situ. In alternative to fluorescent-labeled approaches a new label free method, emerging from the combined utilization of three independent and complementary nanobiotechnological approaches, appears capable to analyze gene and protein function, gene-protein, gene-drug, protein-protein and protein-drug interactions in studies promising for personalized medicine. Quartz Micro Circuit nanogravimetry (QCM), based on frequency and dissipation factor, mass spectrometry (MS) and anodic porous alumina (APA) overcomes indeed the limits of correlated fluorescence detection plagued by the background still present after extensive washes. Work is in progress to further optimize this approach a homogeneous and well defined bacterial cell free expression system able to realize the ambitious objective to quantify the regulatory gene and protein networks in humans. Implications for personalized medicine of the above label free protein array using different test genes and proteins are reported in this PhD thesis