BCIT Citations Collection | BCIT Institutional Repository

BCIT Citations Collection

Pages

Current trends in brain-computer interface research at the Neil Squire foundation
The Neil Squire Foundation (NSF) is a Canadian nonprofit organization whose purpose is to create opportunities for independence for individuals who have significant physical disabilities. Over the last ten years, our team in partnership with researchers at the Electrical and Computer Engineering Department, the University of British Columbia, has been working to develop a direct brain-controlled switch for individuals with significant physical disabilities. The NSF Brain Interface Project primarily focuses on the development of brain-computer interface switch technologies for intermittent (or asynchronous) control in natural environments. That is, technologies that will work when the user intends control but also remains in a stable off state when there is no intent to control. A prototype of such a switch has successfully been developed. This switch has demonstrated classification accuracies greater than 94%. The initial results are promising, but further research is required to improve switch accuracies and reliability and to test these switch technologies over a larger population of users and operating conditions. This paper provides an overview of the NSF brain-switch technologies and details our approach to future work in this area., Peer-reviewed article, Published. Manuscript received June 20, 2002; revised January 22, 2003.
Cyber-Security vulnerabilities: an impediment against further development of Smart Grid
This chapter discusses anomalies which may not be attributed to expected operational deviations and/or mishaps associated with component failure and/or environmental conditions. The question here is: what are known cyber-security vulnerabilities which could be used to aid in the detection of patterns and signatures associated with various types of attacks and intrusions in the system which need to be detected and analyzed using Smart Grid's sensory data, such as Smart meter's and/or PMU's data, to help differentiate between "cyber-attacks in progress" as opposed to "expected system anomalies" due to operational failures of its components?, book chapter, published
Deafferentation and neurotrophin-mediated intraspinal sprouting
Axonal plasticity in the adult spinal cord is governed by intrinsic neuronal growth potential and by extracellular cues. The p75 receptor (p75(NTR)) binds growth-promoting neurotrophins (NTs) as well as the common receptor for growth-inhibiting myelin-derived proteins (the Nogo receptor) and so is well situated to gauge the balance of positive and negative influences on axonal plasticity. Using transgenic mice lacking the extracellular NT-binding domain of p75(NTR) (p75-/- mice), we have examined the influence of p75(NTR) on changes in the density of primary afferent (calcitonin gene-related peptide-expressing) and descending monoaminergic (serotonin- and tyrosine hydroxylase-expressing) projections to the dorsal horn after dorsal rhizotomy, with and without concomitant application of exogenous nerve growth factor and NT-3. We found that, in intact p75-/- mice, the axon density of all populations was equal to or less than that in wild-type mice but that rhizotomy-induced intraspinal sprouting was significantly augmented. Monoaminergic axon sprouting was enhanced in both nerve growth factor- and NT-3-treated p75-/- mice compared with similarly treated wild-type mice. Primary afferent sprouting was particularly robust in NT-3-treated p75-/- mice. These in vivo results illustrate the interactions of p75(NTR) with NTs, with their respective tropomyosin-related kinase receptors and with inhibitory myelin-derived molecules. Our findings illustrate the pivotal role of p75(NTR) in spinal axonal plasticity and identify it as a potential therapeutic target for spinal cord injury., Peer-reviewed article, Published. Received 14 August 2004; Revised 7 October 2004; Accepted 25 October 2004.
A declarative model for reasoning about form security
Proceedings of the International Conference on Agents and Artificial Intelligence in Lisbon, Portugal 2015. We introduce a formal methodology for analysing the security of digital forms, by representing form signing procedures in a declarative action formalism. In practice, digital forms are represented as XML documents and the security of information is guaranteed through the use of digital signatures. However, the security of a form can be compromised in many different ways. For example, an honest agent might be convinced to make a commitment that they do not wish to make or they may be fooled into believing that another agent has committed to something when they have not. In many cases, these attacks do not require an intruder to break any form of encryption or digital signature; instead, the intruder simply needs to manipulate the way signatures are applied and forms are passed between agents. In this paper, we demonstrate that form signing procedures can actually be seen as a variation of the message passing systems used in connection with cryptographic protocols. We start with an exis ting declarative model for reasoning about cryptographic protocols in the Situation Calculus, and we show how it can be extended to identify security issues related to digital signatures, and form signing procedures. We suggest that our results could be used to help users create secure digital forms, using tools such as IBM’s Lotus Forms software., Conference paper, Published.
Design, learn, and play
Proceedings of 2015 Annual Meeting of the American Educational Research Association, Chicago, Illinois, 2015. Evidence suggests that computer game-based learning (GBL) environments are effective in increasing students’ motivation and supporting learning (de Freitas, 2013; Kiili, Ketamo, Koivisto, & Finn, 2014; Spires, Rowe, Mott, & Lester, 2011). Many intelligent tutoring systems and advanced learning technologies are designed as educational games (Aleven, Beal, & Graesser, 2013; Conati, Jaques, & Muir, 2013; Rodrigo, et al., 2012). This paper presents the lessons learned during the design, implementation and evaluation of an educational game, Heroes of Math Island, for students in grades five through seven. The game was designed and implemented with the purpose of researching (1) affective states that are relevant to learning during gameplay and (2) methods that are better suited for design of engaging educational games. This paper focuses on the second objective., Conference paper, Published., Peer reviewed
Design of a dynamic model of genes with multiple autonomous regulatory modules by evolutionary computations
A new approach to design a dynamic model of genes with multiple autonomous regulatory modules by evolutionary computations is proposed. The approach is based on Genetic Algorithms (GA), with new crossover operators especially designed for these purposes. The new operators use local homology between parental strings to preserve building blocks found by the algorithm. The approach exploits the subbasin-portal architecture of the fitness functions suitable for this kind of evolutionary modeling. This architecture is significant for Royal Road class fitness functions. Two real-life Systems Biology problems with such fitness functions are implemented here: evolution of the bacterial promoter rrnP1 and of the enhancer of the Drosophila even-skipped gene. The effectiveness of the approach compared to standard GA is demonstrated on several benchmark and reallife tasks., Peer-reviewed article, Published.
Designing an educational game (Heroes of Math Island)
Proceedings of the 2014 Annual Meeting of the American Educational Research Association, Philadelphia, Pennsylvania. In response to the need for more empirical research with respect to emotion and learning, this study provided an empirical investigation of the students’ interaction with an educational game, Heroes of Math Island, specifically designed for this study. The purpose of this study was to explore learners’ emotional states triggered during gameplay with the goal of providing critical information needed for the design of advanced learning technologies (ALTs) and intelligent tutoring systems (ITSs). The study used the design-based research (DBR) paradigm by combining exploration with design, and mixed methodologies including: pretest, intervention (gameplay), posttest, post-questionnaire, and interview. Fifteen students (seven boys and eight girls) from grades six and seven participated in this study. Findings report on heuristics of educational technology design, emotion, and learning., Conference paper, Published., Peer reviewed
Detection and classification of sensory information from acute spinal cord recordings
One avenue of research for partial restoration of function following spinal cord injury is the use of neural prostheses, an example of which is functional electrical stimulation (FES) devices for motor functions. Neural prostheses may also be useful for the extraction of sensory information directly from the nervous system. We suggest the spinal cord as a possible site for the detection of peripheral sensory information from neural activity alone. Acute multichannel extracellular recordings were used to extract neural spike activity elicited from peripheral sensations from the spinal cords of rats. To test the recording method and classification potential, eight classes of sensory events were recorded consisting of electrical stimulation of seven locations on rat forepaws, and another class of data during which no stimulus was present. A dual-stage classification scheme using principal component analysis and k-Means clustering was devised to classify the sensory events during single trials. The eight tasks were correctly identified at a mean accuracy of 96%. Thus, we have shown the methodology to detect and classify peripheral sensory information from multichannel recordings of the spinal cord. These methods may be useful, for example, in a closed-loop FES for restoration of hand grasp., Peer-reviewed article, Published. Manuscript received October 24, 2005; revised February 25, 2006.
Determination of Aloin A and Aloin B in aloe vera raw materials and finished products by high-performance liquid chromatography
A single-laboratory validation (SLV) was conducted on an HPLC method for the detection and quantification of aloin A and aloin B in Aloe vera raw materials and finished products. An extraction procedure using sonication with an acidified solvent was used for solid test materials while liquid test materials only required dilution, if necessary, prior to filtration and analysis. Separation was achieved using a fused core C18 column in 18 min under isocratic elution conditions allowing for a single analyte (aloin A) calibration curve to quantify both aloins. Adequate chromatographic resolution (Rs ≥ 1) was achieved for aloin A and aloin B. The calibration curves for aloin A exhibited coefficients of determination (r(2)) of ≥ 99.9% over the linear range of 0.3-50 μg/mL. The LOD values were 0.092 and 0.087 μg/mL, and LOQ 0.23 and 0.21 μg/mL for aloin A and aloin B, respectively. Repeatability studies were performed on nine test materials on each of 3 separate days, with five of the test materials determined to be above the LOQ having repeatability RSD (RSDr) values ranging from 0.61 to 6.30%. Method accuracy was determined through a spike recovery study on both liquid and solid matrixes at three different levels: low, medium, and high. For both aloins, the recovery in the liquid matrix ranged from 92.7 to 106.3% with an RSDr of 0.15 to 4.30%, while for the solid matrix, the recovery ranged from 84.4 to 108.9% with an RSDr of 0.23 to 3.84%. Based on the results of the SLV study, it is recommended that this method be evaluated for reproducibility through a collaborative study., Peer-reviewed article, Published. Received January 27, 2013; Accepted by AP April 10, 2014.
Determination of anthocyanins in cranberry fruit and cranberry fruit products by high-performance liquid chromatography with ultraviolet detection
A single-laboratory validation study was conducted on an HPLC method for the detection and quantification of cyanidin-3-O-galactoside (C3Ga), cyanidin-3-O-glucoside (C3GI), cyanidin-3-O-arabinoside (C3Ar), peonidin-3-O-galactoside (P3Ga), and peonidin-3-O-arabinoside (P3Ar) in cranberry fruit (Vaccinium macrocarpon Aiton) raw material and finished products. An extraction procedure using a combination of sonication and shaking with acidified methanol was optimized for all five anthocyanins in freeze-dried cranberry fruit and finished products (commercial extract powder, juice, and juice cocktail). Final extract solutions were analyzed by HPLC using a C18 RP column. Calibration curves for all anthocyanin concentrations had correlation coefficients (r2) of > or = 99.8%. The method detection limits for C3Ga, C3Gl, C3Ar, P3Ga, and P3Ar were estimated to be 0.018, 0.016, 0.006, 0.013, and 0.011 microg/mL, respectively. Separation was achieved with a chromatographic run time of 35 min using a binary mobile phase with gradient elution. Quantitative determination performed in triplicate on four test materials on each of 3 days (n = 12) resulted in RSD(r) from 1.77 to 3.31%. Analytical range, as defined by the calibration curves, was 0.57-36.53 microg/mL for C3Ga, 0.15-9.83 microg/mL for C3GI, 0.28-17.67 microg/mL for C3Ar, 1.01-64.71 microg/mL for P3Ga, and 0.42-27.14 microg/mL for P3Ar. For solid materials prepared by the described method, this translates to 0.06-3.65 mglg for C3Ga, 0.02-0.98 mg/g for C3Gl, 0.03-1.77 mg/g for C3Ar, 0.10-6.47 mg/g for P3Ga, and 0.04-2.71 mg/g for P3Ar., Peer-reviewed article, Published. Received August 5, 2010; Accepted by AP October 27, 2010.
Determination of ginsenoside content in Asian and North American ginseng raw materials and finished products by high-performance liquid chromatography
A single-laboratory validation study was conducted for the quantification of Rg1, Re, Rb1, Rc, Rb2, and Rd in Asian ginseng (Panax ginseng C.A. Meyer) and North American ginseng (Panax quinquefolius L.) raw materials and finished products by RP-HPLC. The extraction with aqueous methanol was optimized for whole root, powdered extract, and finished product (raw, tablet, and capsule matrixes) test articles. Root materials were treated with base to hydrolyze acidic malonyl ginsenosides to their neutral counterparts. Calibration curves for each ginsenoside were linear over the following ranges (microg/g): 5-394 for Rg1, 15-1188 for Re, 39-2981 for Rb1, 6-499 for Rc, 5-406 for Rb2, and 7-600 for Rd, all having a coefficient of determination (r2) of > or = 99.5%. The LOD for Rg1, Re, Rb1, Rc, Rb2, and Rd was determined to be 1.06, 1.25, 2.19, 1.24, 1.27, and 1.70 microg/mL, respectively. Quantitative determinations performed with eight test materials by two analysts over 3 days (n = 12) resulted in RSDr values that ranged from 1.11 to 7.61%., Peer-reviewed article, Published. Received May 10, 2011; Accepted by AP May 11, 2011.
Determination of ginsenoside content in Panax ginseng C.A. Meyer and Panax quinquefolius L. root materials and finished products by high-performance liquid chromatography with ultraviolet absorbance detection
An interlaboratory study was conducted on an HPLC method with UV absorbance detection, previously validated using AOAC single-laboratory validation guidelines, for the determination of the six major ginsenosides (Rg1, Re, Rb1, Rc, Rb2, and Rd) in Panax ginseng C.A. Meyer and Panax quinquefolius L. root materials, extracts, and finished products. Fourteen participating laboratories analyzed five test materials (P. ginseng whole root, P. ginseng powdered extract, P. quinquefolius whole root, P. quinquefolius powdered extract, and P. ginseng powdered extract spiked in a matrix blank) as blind duplicates, and two test materials (P. ginseng powdered whole root tablet and P. quinquefolius powdered extract hard-filled capsule) as single samples. Due to the variability of the ginsenosides (low level concentration of Rb2 in P. quinquefolius raw materials and in P. ginseng spiked matrix blanks, and the possibility of incomplete hydrolysis of the finished products during processing), it was deemed more applicable to analyze total ginsenosides rather than individual ones. Outliers were evaluated and omitted using the Cochran's test and single and double Grubbs' tests. The reproducibility RSD (RSD(R)) for the blind duplicate samples ranged from 4.38 to 5.39%, with reproducibility Horwitz Ratio (HorRat(R)) values ranging from 1.5 to 1.9. For the single replicate samples, the data sets were evaluated solely by their repeatability HorRat (HorRat(r)), which were 2.9 and 3.5 for the capsule and tablet samples, respectively. Based on these results, the method is recommended for AOAC Official First Action for the determination of total ginsenosides in P. ginseng and P. quinquefolius root materials and powdered extracts., Peer-reviewed article, Published.

Pages