Quantitative cardiac magnetic resonance imaging (CMR) has gained traction within both the clinical and research field due to high prevalence of cardiovascular diseases. Cardiac magnetic resonance fingerprinting (cMRF) is a novel approach introduced to address the limitation associated with evaluation of multiparametric quantitative CMR. cMRF enables simultaneous and co-registered estimation of tissue relaxation times, T1 and T2, in a single acquisition, making it a more time-efficient approach to multiparametric quantitative CMR. Nevertheless, cMRF has not gained widespread adaption due to insufficient evidence regarding its performance in accurately quantifying tissue characteristics. This study aims to evaluate the accuracy and reproducibility of a single cMRF sequence described by Hamilton et. al. using self-constructed phantoms to validate the sequence performance for cardiac imaging. The objective was to construct in-vitro phantoms with physiological combinations of T1 and T2 markers. The phantoms were then imaged using gold standard and conventional mapping sequences to establish reference values for comparison. The measurements obtained from the two distinct cMRF reconstruction approaches were then compared to these reference values and to each other to evaluate the accuracy. The statistical assessments did not find a statistically significant difference between neither the cMRF sequence and conventional mapping techniques, nor cMRF and the gold-standard method, when compared in in-vitro phantoms with physiological combinations of T1 and T2. / Kvantitativ kardiovaskulär magnetresonans (CMR) har fått ökad uppmärksamhet inom både den kliniska- och forskningsfältet på grund av hög förekomst av hjärt- och kärlsjukdomar. För att åtgärda begränsningarna vid utvärdering av multiparametrisk kvantitativ CMR, introducerades cardiac magnetic resonance fingerprinting (cMRF) som en ny metod. cMRF möjliggör simultan och samregistrerad uppskattning av vävnadens relaxationstider, T1 och T2, i samma insamling, vilket gör det till en mer tidseffektiv metod för multiparametrisk kvantitativ CMR. Trots detta är kliniska implementeringen av cMRF inte utbredd på grund av otillräckligt bevis för dess utförande vid exakt kvantifiering av vävnadsegenskaper. Syftet med denna studie är att bedöma noggrannheten hos en cMRF-sekvens som utvecklats av Hamilton et al. genom att använda egentillverkade fantomer för att verifiera hur effektiv sekvensen är för avbildning av hjärtat. Målet är att konstruera in vitro-fantom med fysiologiska kombinationer av  T1- och T2-markörer. Dessa fantomer avbildades med hjälp av referensmetoder och konventionell karaktärisering för att etablera jämförelsevärden. Mätningarna som erhölls från de två distinkta cMRF-rekonstruktionsmetoderna jämfördes sedan statistiskt med jämförelsevärdena och med varandra för att utvärdera mätnoggrannheten. De statistiska bedömningarna kunde inte påvisa en skillnad mellan varken cMRF-sekvensen och konventionella metoder, eller referensmetod, vid jämförelse i in vitro-fantom med fysiologiska kombinationer av T1- och T2-värden.

The advent of Storage Class Memory (SCM) is driving a rethink of storage systems towards a single-level architecture where memory and storage are merged. In this context, several works have investigated how to design persistent trees in SCM as a fundamental building block for these novel systems. However, these trees are significantly slower than DRAM-based counterparts since trees are latency-sensitive and SCM exhibits higher latencies than DRAM. In this paper we propose a novel hybrid SCM-DRAM persistent and concurrent B-Tree, named Fingerprinting Persistent Tree (FPTree) that achieves similar performance to DRAM-based counterparts. In this novel design, leaf nodes are persisted in SCM while inner nodes are placed in DRAM and rebuilt upon recovery. The FPTree uses Fingerprinting, a technique that limits the expected number of in-leaf probed keys to one. In addition, we propose a hybrid concurrency scheme for the FPTree that is partially based on Hardware Transactional Memory. We conduct a thorough performance evaluation and show that the FPTree outperforms state-of-the-art persistent trees with different SCM latencies by up to a factor of 8.2. Moreover, we show that the FPTree scales very well on a machine with 88 logical cores. Finally, we integrate the evaluated trees in memcached and a prototype database. We show that the FPTree incurs an almost negligible performance overhead over using fully transient data structures, while significantly outperforming other persistent trees.

Maize is the staple food for a majority of people in Southern Africa, but plant diseases are responsible for at least 10% of crop production losses. Bacterial leaf streak (BLS) of maize was first reported in South Africa in 1949 and has not been reported elsewhere. Very little is known about the pathogen involved and therefore it is deemed necessary to compile a characteristic profile for the pathogen to prevent the possibility of major crop losses as a result of this disease. This study aimed to use biochemical and phenotypic methods to determine the specific characteristics of the causal agent of BLS. Diseased plant material showing symptoms of BLS were collected during the maize production seasons of 2012 and 2013 within South Africa’s maize production regions namely the North West, Free State, Gauteng and Northern Cape provinces. To prevent contamination, maize leaves were surface sterilised thoroughly before bacterial isolation commenced. Sections of the infected maize leaves were placed on GYC agar plates on which yellow, mucoid bacterial colonies after incubation for 24 to 48 hrs. The isolated bacteria were purified and the molecular identification of the bacteria was conducted in a related study. Although literature indicates that Xanthomonas campestris pv. zeae is the causal agent of BLS, pure cultures obtained from maize leaves showing characteristic symptoms of BLS were identified as species of Xanthomonas, Pantoea, and Enterobacter. To elucidate the pathogenicity of the isolated strains, pathogenicity tests based on Koch’s postulates were performed. Results from the pathogenicity tests confirmed that only the isolate Xanthomonas species was capable of inducing the characteristic BLS symptoms when healthy maize plants were inoculated with the suspected pathogens. It is important to inoculate the maize seedlings at the correct age (four-leaf stage) and the spray method is recommended. Re-isolation was repeated from the same plant material used during the initial isolation process but the isolation method was amended. The optimised isolation method involved the use of a dilution range and spread plate method. Colonies from this isolation technique grew as bright yellow colonies that were identified as Xanthomonas spp. This outcome indicates the importance of surface sterilisation, pulverisation and subsequent dilution of plant materials for isolation of bacterial pathogens from diseases plants. These isolates were used to create protein profiles with SDS-PAGE electrophoresis and carbon utilisation patterns with the Biolog® GN2 system. Protein profiling banding patterns was assessed based on presence/absence criteria. Highly similar protein profiles were observed among the X. campestris pv. zeae isolates but groupings of different protein profiles were determined when minor differences in the protein profiles was taken into account. Xanthomonas campestris pv. zeae was successfully distinguished from the X. axonopodis pv. vasculorum reference strain through unique SDS banding patterns. Banding patterns obtained from cultures grown in a liquid medium (tryptic soy broth) were of a higher quality than the banding patterns obtained from bacteria harvested from solid media (CYG agar plates). Carbon source utilisation data was used to evaluate the average well colour development obtained from each isolate. Statistically significant differences were found among some of the isolates, with some isolates being metabolically more active than other isolates. Substrate utilisation patterns produced by the isolates corresponded to previously published studies on various Xanthomonas species. The cell count of the samples used during carbon utilisation patterns must be standardised in order to obtain reliable results. During this study, the application of Koch’s postulates and two inoculation techniques confirmed that Xanthomonas campestris pv. zeae is the pathogen responsible for bacterial leaf streak of maize. Members of the Pantoea and Enterobacter genera were found on the leaf surface of maize plants infected with BLS but inoculations of healthy maize plants with these bacteria did not result in bacterial leaf streak symptoms on the maize plants. These bacteria were not pathogenic and were considered endophytes. The identified pathogen was characterised through protein and metabolic profiling. The protein profiles of the pathogen obtained through analysis of the major bands of the SDS-PAGE gels were highly similar and distinguishable from the Xanthomonas reference culture. Groupings within the X. campestris pv. zeae group was found when major and minor bands were considered, this may however be altered when the intensities of the bands are used during analysis. Carbon utilisation patterns were assessed using Biolog® GN2 plates. A metabolic fingerprint was created for the pathogen of BLS, it was possible to distinguish between X. campestris pv. zeae and other Xanthomonas strains based on the fingerprint. This fingerprint could be used to identify the pathogen. / MSc (Environmental Sciences), North-West University, Potchefstroom Campus, 2015

Maize is the staple food for a majority of people in Southern Africa, but plant diseases are responsible for at least 10% of crop production losses. Bacterial leaf streak (BLS) of maize was first reported in South Africa in 1949 and has not been reported elsewhere. Very little is known about the pathogen involved and therefore it is deemed necessary to compile a characteristic profile for the pathogen to prevent the possibility of major crop losses as a result of this disease. This study aimed to use biochemical and phenotypic methods to determine the specific characteristics of the causal agent of BLS. Diseased plant material showing symptoms of BLS were collected during the maize production seasons of 2012 and 2013 within South Africa’s maize production regions namely the North West, Free State, Gauteng and Northern Cape provinces. To prevent contamination, maize leaves were surface sterilised thoroughly before bacterial isolation commenced. Sections of the infected maize leaves were placed on GYC agar plates on which yellow, mucoid bacterial colonies after incubation for 24 to 48 hrs. The isolated bacteria were purified and the molecular identification of the bacteria was conducted in a related study. Although literature indicates that Xanthomonas campestris pv. zeae is the causal agent of BLS, pure cultures obtained from maize leaves showing characteristic symptoms of BLS were identified as species of Xanthomonas, Pantoea, and Enterobacter. To elucidate the pathogenicity of the isolated strains, pathogenicity tests based on Koch’s postulates were performed. Results from the pathogenicity tests confirmed that only the isolate Xanthomonas species was capable of inducing the characteristic BLS symptoms when healthy maize plants were inoculated with the suspected pathogens. It is important to inoculate the maize seedlings at the correct age (four-leaf stage) and the spray method is recommended. Re-isolation was repeated from the same plant material used during the initial isolation process but the isolation method was amended. The optimised isolation method involved the use of a dilution range and spread plate method. Colonies from this isolation technique grew as bright yellow colonies that were identified as Xanthomonas spp. This outcome indicates the importance of surface sterilisation, pulverisation and subsequent dilution of plant materials for isolation of bacterial pathogens from diseases plants. These isolates were used to create protein profiles with SDS-PAGE electrophoresis and carbon utilisation patterns with the Biolog® GN2 system. Protein profiling banding patterns was assessed based on presence/absence criteria. Highly similar protein profiles were observed among the X. campestris pv. zeae isolates but groupings of different protein profiles were determined when minor differences in the protein profiles was taken into account. Xanthomonas campestris pv. zeae was successfully distinguished from the X. axonopodis pv. vasculorum reference strain through unique SDS banding patterns. Banding patterns obtained from cultures grown in a liquid medium (tryptic soy broth) were of a higher quality than the banding patterns obtained from bacteria harvested from solid media (CYG agar plates). Carbon source utilisation data was used to evaluate the average well colour development obtained from each isolate. Statistically significant differences were found among some of the isolates, with some isolates being metabolically more active than other isolates. Substrate utilisation patterns produced by the isolates corresponded to previously published studies on various Xanthomonas species. The cell count of the samples used during carbon utilisation patterns must be standardised in order to obtain reliable results. During this study, the application of Koch’s postulates and two inoculation techniques confirmed that Xanthomonas campestris pv. zeae is the pathogen responsible for bacterial leaf streak of maize. Members of the Pantoea and Enterobacter genera were found on the leaf surface of maize plants infected with BLS but inoculations of healthy maize plants with these bacteria did not result in bacterial leaf streak symptoms on the maize plants. These bacteria were not pathogenic and were considered endophytes. The identified pathogen was characterised through protein and metabolic profiling. The protein profiles of the pathogen obtained through analysis of the major bands of the SDS-PAGE gels were highly similar and distinguishable from the Xanthomonas reference culture. Groupings within the X. campestris pv. zeae group was found when major and minor bands were considered, this may however be altered when the intensities of the bands are used during analysis. Carbon utilisation patterns were assessed using Biolog® GN2 plates. A metabolic fingerprint was created for the pathogen of BLS, it was possible to distinguish between X. campestris pv. zeae and other Xanthomonas strains based on the fingerprint. This fingerprint could be used to identify the pathogen. / MSc (Environmental Sciences), North-West University, Potchefstroom Campus, 2015

With the increasing use of the Internet several problems have arisen regarding the processing of electronic documents. These include content filtering, content retrieval/search. Moreover, document security has taken a centre stage including copyright protection, broadcast monitoring etc. There is an acute need of an effective tool which can find the identity, location and the time when the document was created so that it can be determined whether or not the contents of the document were tampered with after creation. Owing the sensitivity of the large amounts of data which is processed on a daily basis, verifying the authenticity and integrity of a document is more important now than it ever was. Unsurprisingly document authenticity verification has become the centre of attention in the world of research. Consequently, this research is concerned with creating a tool which deals with the above problem. This research proposes the use of a Quick Response Code as a message carrier for Text Key-print. The Text Key-print is a novel method which employs the basic element of the language (i.e. Characters of the alphabet) in order to achieve authenticity of electronic documents through the transformation of its physical structure into a logical structured relationship. The resultant dimensional matrix is then converted into a binary stream and encapsulated with a serial number or URL inside a Quick response Code (QR code) to form a digital fingerprint mark. For hiding a QR code, two image steganography techniques were developed based upon the spatial and the transform domains. In the spatial domain, three methods were proposed and implemented based on the least significant bit insertion technique and the use of pseudorandom number generator to scatter the message into a set of arbitrary pixels. These methods utilise the three colour channels in the images based on the RGB model based in order to embed one, two or three bits per the eight bit channel which results in three different hiding capacities. The second technique is an adaptive approach in transforming domain where a threshold value is calculated under a predefined location for embedding in order to identify the embedding strength of the embedding technique. The quality of the generated stego images was evaluated using both objective (PSNR) and Subjective (DSCQS) methods to ensure the reliability of our proposed methods. The experimental results revealed that PSNR is not a strong indicator of the perceived stego image quality, but not a bad interpreter also of the actual quality of stego images. Since the visual difference between the cover and the stego image must be absolutely imperceptible to the human visual system, it was logically convenient to ask human observers with different qualifications and experience in the field of image processing to evaluate the perceived quality of the cover and the stego image. Thus, the subjective responses were analysed using statistical measurements to describe the distribution of the scores given by the assessors. Thus, the proposed scheme presents an alternative approach to protect digital documents rather than the traditional techniques of digital signature and watermarking.

Received Signal Strength Indication (RSSI) fingerprinting is a popular technique in the fieldof indoor positioning. Many studies on the subject exist acknowledging Wi-Fi signal variationconnected to Wi-Fi signals, but does not discuss possible signal variation created byconnected devices nor consequential precision loss.Understanding more about the origins of signal variation in received signal strength indication(RSSI) fingerprinting would help deal with or prevent them as well as provide moreknowledge for applications based on such signals. Environments with a varying number ofconnected devices would benefit from knowing changes in localization precision resultingfrom the devices connecting and disconnecting from the access point because it wouldindicate whether workarounds for such circumstances would be necessary.To address this issue, the work presented here focuses on how the precision of RSSIfingerprinting vary given different levels of connected Wi-Fi devices. It was carried out byconducting real world experiments at times of low- and normal levels of connected devices toaccess points on two separate locations and evaluating precision changes between statedactivity levels. These experiments took place at the University of Borås as well as at Ericssonin Borås.Experimental findings indicate that the accuracy does deteriorate in higher levels of activitythan in low activity, even though not enough evidence to determine the precision ofdeterioration. The experiments thereby provide a foundation for location-based applicationsand services that can communicate the level of positional error that exist in differentenvironments which would make the users aware but also make the applications adaptaccordingly to different environments. Based on the precision achieved, we identify variousapplications that would benefit from our proposed model. These were applications that wouldtrack mobile resources, find immobile resources, find the movement flows of users as well asnavigation- and Wi-Fi coverage applications.Further research for investigating the exact correlation between access point stress andprecision loss is proposed to fully understand the implications connected devices have onRSSI fingerprinting.

Forensic STR analysis is limited by the quality and quantity of DNA. Significant damage or alteration to the molecular structure of DNA by depurination, crosslinking, base modification, and strand breakage can impact typing success. Two methods that could potentially improve STR typing of challenged samples were explored: an in vitro DNA repair assay (PreCR™ Repair Mix) and whole genome amplification. Results with the repair assay showed trends of improved performance of STR profiling of bleach-damaged DNA. However, the repair assay did not improve DNA profiles from environmentally-damaged bloodstains or bone, and in some cases resulted in lower RFU values for STR alleles. The extensive spectrum of DNA damage and myriad combinations of lesions that can be present in forensic samples appears to pose a challenge for the in vitro PreCR™ assay. The data suggest that the use of PreCR™ in casework should be considered with caution due to the assay’s varied results. As an alternative to repair, whole genome amplification (WGA) was pursued. The DOP-PCR method was selected for WGA because of initial primer design and greater efficacy for amplifying degraded samples. Several modifications of the original DOP-PCR primer were evaluated. These modifications allowed for an overall more robust amplification of damaged DNA from both contemporary and historical skeletal remains compared with that obtained by standard DNA typing and a previously described DOP-PCR method. These new DOP-PCR primers show promise for WGA of degraded DNA.

L’esca est une maladie de dépérissement du bois de la vigne conduisant à la mort des ceps. Actuellement le vignoble mondial est atteint, et au niveau français, cette maladie ne cesse de progresser. Ainsi, 8% des ceps dans le Jura et 4,5% dans la région de Bordeaux manifestent des symptômes d’esca, selon les parcelles des chiffres beaucoup plus élevés sont obtenus, certains cépages sont aussi beaucoup plus sensibles que d’autres. Plusieurs champignons seraient impliqués dans l’esca mais leur rôle ainsi que la détermination de la microflore responsable de cette maladie est encore sujette à interrogation. Dans ce contexte, l’objectif de cette thèse a été de caractériser et de comparer les microflores fongiques et bactériennes colonisant le bois de ceps de vigne ayant exprimé ou non des symptômes foliaires d’esca. Dans un premier temps, nous avons prélevé des ceps (cultivar Cabernet Sauvignon) relativement jeunes (10 ans d’âge) car ils présentaient l’intérêt d’être peu dégradés au niveau du bois du tronc, les symptômes foliaires étant associés à la présence d’amadou (une nécrose typique de l’esca) uniquement dans les bras. Une grande diversité dans les communautés fongiques (674 OTUs) et bactériennes (222 OTUs) colonisant le bois a été observée. Cette diversité est plus importante dans le bois sain de la vigne que dans celui partiellement ou totalement nécrosé. Les techniques utilisées, i.e. isolement/séquençage de souches, empreinte moléculaire (Single Strand Conformation Polymorphism, SSCP) et pyroséquençage 454, ont montré que les communautés bactériennes ou fongiques étaient différentes dans les tissus dégradés comparés à ceux qui ne l’étaient pas. Des changements de microflores en fonction du temps (expérimentation durant 1 année) ont aussi été observés. D’une façon générale, les espèces de champignons impliquées dans l’esca sont déjà présentes dans le bois apparemment sain de ceps esca-foliaires symptomatiques mais aussi des asymptomatiques. Il n’a pas été possible de différencier ces 2 types de microflores au niveau du bois sain des plants, cette différentiation se faisant au niveau des nécroses, qui sont plus abondantes dans les ceps esca-symptomatiques. Pour la première fois nous avons montré que des communautés bactériennes spécifiques étaient associées à l’esca, leurs aptitudes trophiques étant différentes selon les tissus où elles étaient prélevées. Les espèces isolées suggèrent que certaines pourraient avoir un rôle dans la protection du végétal, d’autres dans la dégradation des structures du bois, e.g. de la lignine, préparant ainsi le terrain aux champignons dégradateurs des tissus ligneux, déjà présents à l’intérieur des ceps. Nous avons aussi étudiés des ceps plus âgés (cultivar Baco blanc), de 42 et 58 ans, qui avaient un rendement acceptable et n’avaient pas manifesté de symptômes d’esca ou eutypiose (une autre maladie du bois) l’année du prélèvement. Au niveau des tissus fonctionnels du bois, les communautés fongiques étaient caractéristiques de plants atteints par l’eutypiose (ceps de 42 ans) ou de l’esca (ceux de 58 ans). La non expression par les ceps de ces 2 maladies pourrait cependant être associée à la forte présence de champignons mycoparasites et protecteur du végétal, comme Trichoderma spp., dans ces tissus fonctionnels. Les interactions au sein des communautés fongiques créant un équilibre où le pathogène ne se développerait pas de façon extensive. Les caractéristiques du Baco blanc, un hybride, moins sensible à certaines maladies de la vigne, pourrait aussi expliquer ce résultat. Ainsi la présence d’une microflore bénéfique naturellement présente dans le bois des ceps associée à des plants ayant une tolérance à ces maladies pourrait ouvrir de nouvelles perspectives pour lutter l’esca, voire l’eutypiose, pour lesquelles aucun moyen de protection n’existe aujourd’hui. / Esca is a Grapevine Trunk Disease (GTD) that induces a decline in grapevine vigour that generally leads up with the death of the plants. Nowadays, vineyards worldwide are attacked by esca and, in France this disease increases steadily. In the Jura, 8% of the grapevines are esca-foliar symptomatic and approximately 4.5% in the Bordeaux region. However, some vineyards are more severely attacked by esca, and certain cultivars are more susceptible than others. Although several pathogenic fungi are associated with esca, their individual roles and their interaction with other microorganisms for the esca have still to be determined. In this context, the objective of the present PhD study is to characterize and compare the bacterial and fungal microflora that colonize the wood tissues of esca-foliar symptomatic and asymptomatic grapevines. First, we sampled young (10 year-old) grapevines (Cabernet Sauvignon cultivar) because they had only few necroses in the trunk and white-rot (also called amadou) was only present in the cordons of symptomatic plants. Great diversity in the fungal (674 OTUs) and bacterial (222 OTUs) communities was observed. This diversity was higher in the apparently healthy wood than in the partially or totally necrotic wood tissues. The methods used isolation/sequencing of microbial strains, a molecular fingerprinting method (Single Strand Conformation Polymorphism, SSCP) and 454 pyrosequencing showed that the fungal and bacterial communities of the necrotic and healthy wood tissues were different. Changes in the microflora over time (over a one-year period) have been observed. Fungal species involved in esca are already present in the apparently healthy wood of esca-foliar symptomatic plants but also in the asymptomatic ones. It was not possible to differentiate these 2 microflora. Only microflora from the necroses differed from those of the healthy wood with these necroses being more developed in the esca-foliar symptomatic grapevines. For the first time, we were able to determine that specific bacterial communities are associated with esca. Depending on the wood tissues, different types of bacteria were isolated, with different trophic behaviour. Two roles could be assigned to the species isolated from the various wood tissues: (i) a positive role, due to the biocontrol potential that many species have; (ii) a negative one, by predisposing the wood of grapevines to fungal attacks. We also studied, old (42 and 58 year-old) grapevines of the cultivar, Baco blanc, that produced regular harvests. The plants had no expressed foliar symptoms of esca or eutypa dieback during the sampling year. Many plant pathogens colonized the functional wood tissues, but in 58 year-old plants they were associated with esca, and in 42 year-old plants, with eutypa dieback. The absence of GTDs expression could be linked to the numerous plant protectant mycoparasites, such as Trichoderma spp., that colonized the functional wood tissues. Interactions between species within the fungal communities may create a balance that is unfavourable to the development of the pathogens. The use of Baco blanc, a hybrid less susceptible to certain grapevine diseases could also explain this result. So, because no means of protection are currently available, the combination of beneficial microflora within the garpevine wood tissues with plants that are tolerant to esca, or even eutypa dieback, could be helpful to control those diseases.

Recently, there has been an enormous growth of interests in geolocation applications that demand an accurate estimation of the user’s location in indoor areas. The traditional geolocation system, GPS, which was designed for being used in outdoor environments, does not perform well in indoor areas, causing frequent inaccuracies in location estimation. Therefore the need for more accurate positioning systems and even positioning techniques is a motivation for researchers to turn their attention into indoor positioning systems. In this thesis we present a unique testbed for indoor geolocation system’s real-time performance evaluation. Then we present a real-time performance evaluation of a sample indoor positioning system. We make a comparison between the simulated results of the performance evaluation of the positioning engine and the real-time performance evaluation of the positioning system. Finally, we perform a sensitivity analysis for Ekahauâ„¢ indoor positioning engine. We show that the simulation with the introduced testbed yields the same results as one would obtain by evaluating the performance of the positioning system by means of massive measurement campaigns. Running the testbed for several measurement campaigns for different scenarios enabled us to compare the results and study the effect of selected parameters on the performance of the positioning system. We also perform primitive error analysis in terms of distance error to verify the validity of the result obtained with the testbed. We show that under the same configuration both real-time performance evaluation and simulated performance evaluation will yield same result with respect to position error. We also use error modeling to determine which error model is best matched to the observed indoor positioning error. Amongst all of the possibilities of choosing methods of positioning, we focused on the Received Signal Strength (RSS) based method along with fingerprinting. Briefly said, profiles previously gathered by measurement or simulation will decide on the location of mobile terminal if a new profile comes in. It is worth mentioning that previous work similar to this testbed has been done for outdoor areas according to Ekahau's white paper. Their work is mainly focused on outdoor environment, in which multipath does not exist. In this research effort we tried to analyze the effect of different parameters on sensitivity of indoor positioning systems who suffer from multipath. Different setups for simulating real-time radio channels have been studied in literature, but still not focused on indoor areas.

The ability of jurors and juries to comprehend and utilise scientific evidence in Australian criminal trials has been examined. From mock jury surveys relating to DNA profiling evidence, it was determined that most respondents were able to comprehend some basic and applied statistics, although their ability was in part related to their knowledge of English and their level of education. The point at which mock jurors were prepared to convict an accused solely on the basis of DNA profiling evidence was examined and found to be low compared with the strength of DNA profiling evidence commonly presented in Australian courts. Mock jurors also demonstrated the ability to process evidence that was presented in a Bayesian framework; commencing with prior odds, introducing new information and culminating in posterior odds. From a survey of Australian forensic scientists, including fraud investigators, it was found that most practitioners' concerns could be addressed by greater pre-trial consultation between experts and legal advocates. Improved knowledge within the legal profession concerning the jargon, principles, procedures, limitations and conclusions to be drawn from different scientific disciplines, prior to presenting this evidence in court, is recommended as the means by which complex evidence can be better adduced from expert witnesses and better presented to juries in criminal trials. Finally, from interviewing actual jurors in criminal trials in the Australian Capital Territory it was determined that where jurors' expectations of scientific evidence, particularly DNA profiling evidence, are not met, high levels of juror frustration and speculation may culminate in hung juries. The adversarial setting of criminal proceedings was also found to produce an environment in which jurors felt that information that would assist them in reaching a verdict was being deliberately withheld. The ability of the jury to ask questions and the allowed nature of those questions were also examined, with the resultant recommendation that juries be given more explicit information at the commencement of trials to inform them about their rights and obligations when asking questions.