004 Datenverarbeitung; Informatik
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Principles of cognitive maps
(2021)
This thesis analyses the concept of a cognitive map in the research fields of geography. Cognitive mapping research is essential as it investigates the relations between cognitive maps and external representations of space that people regularly use by acquiring spatial knowledge, such as maps in geographic information systems. Moreover, cognitive maps, when expanded on semantic maps, explain the relations between people and things in a non-physically environment, where the considered space is not spanned by distance but with other non-spatially variables. Nevertheless, cognitive maps are often distorted. Although a good formation of a cognitive map is vital in navigation processes, cognitive distortions are barely investigated in the field of geography. By analyzing the relevant work, especially Tobler’s first law of geography, a new lexical variant of Tobler’s first law could be stated that could presumably describe a specific distortion in the processing of landmarks in cognitive maps.
At present, there are no quantitative, objective methods for diagnosing the Parkinson disease. Existing methods of quantitative analysis by myograms suffer by inaccuracy and patient strain; electronic tablet analysis is limited to the visible drawing, not including the writing forces and hand movements. In our paper we show how handwriting analysis can be obtained by a new electronic pen and new features of the recorded signals. This gives good results for diagnostics. Keywords: Parkinson diagnosis, electronic pen, automatic handwriting analysis
Modern experiments in heavy ion collisions operate with huge data rates that can not be fully stored on the currently available storage devices. Therefore the data flow should be reduced by selecting those collisions that potentially carry the information of the physics interest. The future CBM experiment will have no simple criteria for selecting such collisions and requires the full online reconstruction of the collision topology including reconstruction of short-lived particles.
In this work the KF Particle Finder package for online reconstruction and selection of short-lived particles is proposed and developed. It reconstructs more than 70 decays, covering signals from all the physics cases of the CBM experiment: strange particles, strange resonances, hypernuclei, low mass vector mesons, charmonium, and open-charm particles.
The package is based on the Kalman filter method providing a full set of the particle parameters together with their errors including position, momentum, mass, energy, lifetime, etc. It shows a high quality of the reconstructed particles, high efficiencies, and high signal to background ratios.
The KF Particle Finder is extremely fast for achieving the reconstruction speed of 1.5 ms per minimum-bias AuAu collision at 25 AGeV beam energy on single CPU core. It is fully vectorized and parallelized and shows a strong linear scalability on the many-core architectures of up to 80 cores. It also scales within the First Level Event Selection package on the many-core clusters up to 3200 cores.
The developed KF Particle Finder package is a universal platform for short- lived particle reconstruction, physics analysis and online selection.
Artificial Intelligence (AI) has the potential to greatly improve the delivery of healthcare and other services that advance population health and wellbeing. However, the use of AI in healthcare also brings potential risks that may cause unintended harm. To guide future developments in AI, the High-Level Expert Group on AI set up by the European Commission (EC), recently published ethics guidelines for what it terms “trustworthy” AI. These guidelines are aimed at a variety of stakeholders, especially guiding practitioners toward more ethical and more robust applications of AI. In line with efforts of the EC, AI ethics scholarship focuses increasingly on converting abstract principles into actionable recommendations. However, the interpretation, relevance, and implementation of trustworthy AI depend on the domain and the context in which the AI system is used. The main contribution of this paper is to demonstrate how to use the general AI HLEG trustworthy AI guidelines in practice in the healthcare domain. To this end, we present a best practice of assessing the use of machine learning as a supportive tool to recognize cardiac arrest in emergency calls. The AI system under assessment is currently in use in the city of Copenhagen in Denmark. The assessment is accomplished by an independent team composed of philosophers, policy makers, social scientists, technical, legal, and medical experts. By leveraging an interdisciplinary team, we aim to expose the complex trade-offs and the necessity for such thorough human review when tackling socio-technical applications of AI in healthcare. For the assessment, we use a process to assess trustworthy AI, called 1Z-Inspection® to identify specific challenges and potential ethical trade-offs when we consider AI in practice.
Co-design of a trustworthy AI system in healthcare: deep learning based skin lesion classifier
(2021)
This paper documents how an ethically aligned co-design methodology ensures trustworthiness in the early design phase of an artificial intelligence (AI) system component for healthcare. The system explains decisions made by deep learning networks analyzing images of skin lesions. The co-design of trustworthy AI developed here used a holistic approach rather than a static ethical checklist and required a multidisciplinary team of experts working with the AI designers and their managers. Ethical, legal, and technical issues potentially arising from the future use of the AI system were investigated. This paper is a first report on co-designing in the early design phase. Our results can also serve as guidance for other early-phase AI-similar tool developments.
Poster presentation A central problem in neuroscience is to bridge local synaptic plasticity and the global behavior of a system. It has been shown that Hebbian learning of connections in a feedforward network performs PCA on its inputs [1]. In recurrent Hopfield network with binary units, the Hebbian-learnt patterns form the attractors of the network [2]. Starting from a random recurrent network, Hebbian learning reduces system complexity from chaotic to fixed point [3]. In this paper, we investigate the effect of Hebbian plasticity on the attractors of a continuous dynamical system. In a Hopfield network with binary units, it can be shown that Hebbian learning of an attractor stabilizes it with deepened energy landscape and larger basin of attraction. We are interested in how these properties carry over to continuous dynamical systems. Consider system of the form Math(1) where xi is a real variable, and fi a nondecreasing nonlinear function with range [-1,1]. T is the synaptic matrix, which is assumed to have been learned from orthogonal binary ({1,-1}) patterns ξμ, by the Hebbian rule: Math. Similar to the continuous Hopfield network [4], ξμ are no longer attractors, unless the gains gi are big. Assume that the system settles down to an attractor X*, and undergoes Hebbian plasticity: T´ = T + εX*X*T, where ε > 0 is the learning rate. We study how the attractor dynamics change following this plasticity. We show that, in system (1) under certain general conditions, Hebbian plasticity makes the attractor move towards its corner of the hypercube. Linear stability analysis around the attractor shows that the maximum eigenvalue becomes more negative with learning, indicating a deeper landscape. This in a way improves the system´s ability to retrieve the corresponding stored binary pattern, although the attractor itself is no longer stabilized the way it does in binary Hopfield networks.
Contemporary information systems make widespread use of artificial intelligence (AI). While AI offers various benefits, it can also be subject to systematic errors, whereby people from certain groups (defined by gender, age, or other sensitive attributes) experience disparate outcomes. In many AI applications, disparate outcomes confront businesses and organizations with legal and reputational risks. To address these, technologies for so-called “AI fairness” have been developed, by which AI is adapted such that mathematical constraints for fairness are fulfilled. However, the financial costs of AI fairness are unclear. Therefore, the authors develop AI fairness for a real-world use case from e-commerce, where coupons are allocated according to clickstream sessions. In their setting, the authors find that AI fairness successfully manages to adhere to fairness requirements, while reducing the overall prediction performance only slightly. However, they find that AI fairness also results in an increase in financial cost. Thus, in this way the paper’s findings contribute to designing information systems on the basis of AI fairness.
With free delivery of products virtually being a standard in E-commerce, product returns pose a major challenge for online retailers and society. For retailers, product returns involve significant transportation, labor, disposal, and administrative costs. From a societal perspective, product returns contribute to greenhouse gas emissions and packaging disposal and are often a waste of natural resources. Therefore, reducing product returns has become a key challenge. This paper develops and validates a novel smart green nudging approach to tackle the problem of product returns during customers’ online shopping processes. We combine a green nudge with a novel data enrichment strategy and a modern causal machine learning method. We first run a large-scale randomized field experiment in the online shop of a German fashion retailer to test the efficacy of a novel green nudge. Subsequently, we fuse the data from about 50,000 customers with publicly-available aggregate data to create what we call enriched digital footprints and train a causal machine learning system capable of optimizing the administration of the green nudge. We report two main findings: First, our field study shows that the large-scale deployment of a simple, low-cost green nudge can significantly reduce product returns while increasing retailer profits. Second, we show how a causal machine learning system trained on the enriched digital footprint can amplify the effectiveness of the green nudge by “smartly” administering it only to certain types of customers. Overall, this paper demonstrates how combining a low-cost marketing instrument, a privacy-preserving data enrichment strategy, and a causal machine learning method can create a win-win situation from both an environmental and economic perspective by simultaneously reducing product returns and increasing retailers’ profits.
Neuropsychiatric disorders are complex, highly heritable but incompletely understood disorders. The clinical and genetic heterogeneity of these disorders poses a significant challenge to the identification of disorder related biomarkers. Besides significant progress in unveiling the genetic basis of these disorders, the underlying causes and biological mechanisms remain obscure. With the advancement in the array, sequencing, and big data technologies, a huge amount of data is generated from individuals across different platforms and in various data structures. But there is a paucity of bioinformatics tools that can integrate this plethora of data. Therefore, there is a need to develop an integrative bioinformatics data analysis tool that combines biological and clinical data from different data types to better understand the underlying genetics.
This thesis presents a bioinformatics pipeline implementing data from different platforms to provide a thorough understanding of the genetic etiology of a neuropsychiatric quantitative as well as a qualitative trait of interest. Throughout the thesis, we present two aspects: one is the development and architecture of the bioinformatics pipeline named MApping the Genetics of neuropsychiatric traits to the molecular NETworks of the human brain (MAGNET). The other part demonstrates the implementation and usefulness of MAGNET analysing large Autism Spectrum Disorder (ASD) cohorts.
MAGNET is a freely available command-line tool available on GitHub (https://github.com/SheenYo/MAGNET). It is implemented within one framework using data integration approaches based on state-of-the-art algorithms and software to ultimately identify the genes and pathways genetically associated with a trait of interest. MAGNET provides an edge over the existing tools since it performs a comprehensive analysis taking care of the data handling and parsing steps necessary to communicate between the different APIs (Application Program Interface). Thus, this avoids the in-between data handling steps required by researchers to provide output from one analysis to the next. Moreover, depending on the size of the dataset users can deduce important information regarding their trait of interest within a time frame of a few days. Besides gaining insights into genetic associations, one of the central features is the mapping of the associated genes onto developing human brain implementing transcriptome data of 16 different brain regions starting from the 5th post-conceptional week to over 40 years of age.
In the second part as proof of concept, we implemented MAGNET on two ASD cohorts. ASD is a group of psychiatric disorders. Clinically, ASD is characterized by the following psychopathology: A) limitations in social interaction and communication, and B) restricted, repetitive behavior. The etiology of this disorder is extremely complex due to its heterogeneous clinical traits and genetics. Therefore, to date, no reliable biomarkers are identified. Here, the aim is to characterize the genetic architecture of ASD taking into account the two aforementioned ASD diagnostic domains. As well as to investigate if these domains are genetically linked or independent of each other. Moreover, we addressed the question if these traits share genetic risk with the categorical diagnosis of ASD and how much of the phenotypic variance of these traits can be explained by the underlying genetics.
We included affected individuals from two ASD cohorts, i.e. the Autism Genome Project (AGP) and a German cohort consisting of 2,735 and 705 families respectively. MAGNET was applied to each of the ASD subdomains as a quantitative dependent variable. MAGNET is divided into five main sections i.e. (1) quality check of the genotype data, (2) imputation of missing genotype data, (3) association analysis of genotype and trait data, (4) gene-based analysis, and (5) enrichment analysis using gene expression data from the human brain.
MAGNET was applied to each of the individual traits in each cohort to perform quality control of the genetic data and imputed the missing data in an automated fashion. MAGNET identified 292 known and new ASD risk genes. These genes were subsequently assigned to biological signaling pathways and gene ontologies via MAGNET. The underlying biological mechanisms converged with respect to neuronal transmission and development processes. By reconciling these genes with the transcriptome of the developing human brain, MAGNET was able to identify that the significant genes associated with the subdomains are expressed at specific time points in brain areas such as the hippocampus, amygdala, and cortical regions. Further, we found that ASD subdomains related to domain A but not
to domain B have a shared genetic etiology.