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Aside from hardware, a major component of a Brain Computer Interface is the software that provides the tools for translating raw acquired brain signals into commands to control an application or a device. There’s a range of software, some proprietary, like MATLAB and some free and open source (FOSS), accessible under the GNU General Public License (GNU GPL). OpenViBE is one such freely accessible software. This thesis carries out a functionality and usability test of the platform, looking at its portability, architecture and communication protocols. To investigate the feasibility of reproducing the P300 xDAWN speller BCI presented by OpenViBE, users focused on a character on a 6x6 alphanumeric grid which contained a sequence of random flashes of the rows and columns. Visual stimulus is presented to a user every time the character they are focusing on is highlighted in a row or column. A TMSi analog-to-digital converter was used together with a 32-channel active electrode cap (actiCAP) to record user’s Electroencephalogram (EEG) which was then used in an offline session to train the spatial filter algorithm, and the classifier to identify the P300 evoked potentials, elicited as a user’s reaction to an external stimulus. In an online session, the users tried to spell with the application using the power of their brain signal. Aspects of evoked potentials (EP), both auditory (AEP) and visual (VEP) are further investigated as a validation of results of the P300 speller.
Cytoscape is an open source platform for complex network analysis and visualisation. The Pathway Interaction Database (PID) is a highly structured, curated collection of information about known biomolecular interactions and key cellular processes assembled into signalling pathways. Despite the obvious potential and advantageous usage of both tool (Cytoscape) and information source (PID), there has been no conclusive effort to merge and synergise them. This project aims to make use of the open source characteristics of Cytoscape and optimally visualise the biomolecular interactions found in the PID. This is made possible by the development of a plugin which imports a user-selected pathway file, converts it into a Cytoscape-readable file, and then visualises it. Finally, the user has options to further optimise the pathway by the use of a filter (Barcode – Affymetrix) that removes nodes from the network which are lowly expressed in the Affymetrix microarray data. The user then obtains visual results in a matter of seconds. Additionally, the process of subgraphing nodes through the shortest path method could be applied to the network. This can further assist the user in identifying the molecular pathways of the nodes of interest, a useful feature in network analysis.
Medication reconciliation is defined by the American Society of Health- System Pharmacists (ASHP) and the American Pharmacists Association (AphA) as “the comprehensive evaluation of a patient’s medication regimen any time there is a change in therapy in an effort to avoid medication errors such as omissions, duplications, dosing errors or drug interactions, as well as to observe compliance and adherence patterns “. Medication reconciliation is very important to avoid medication errors but it is also a complex and time-consuming process. Medication histories, i.e. records of prescription, purchase, and refill sequences are considered to be a resource from which conclusions about medication reconciliation can be drawn. However, medication histories spread across diverse paper and electronic media may lack the required accuracy. By employing multiple electronic sources this thesis will evaluate if more accurate medication histories can be collected.