Prof. Dr.-Ing. Andreas Maier

Prof. Dr. Andreas Maier was born on 26th of November 1980 in Erlangen. He studied Computer Science, graduated in 2005, and received his PhD in 2009. From 2005 to 2009 he was working at the Pattern Recognition Lab at the Computer Science Department of the University of Erlangen-Nuremberg. His major research subject was medical signal processing in speech data. In this period, he developed the first online speech intelligibility assessment tool - PEAKS - that has been used to analyze over 4.000 patient and control subjects so far.

From 2009 to 2010, he started working on flat-panel C-arm CT as post-doctoral fellow at the Radiological Sciences Laboratory in the Department of Radiology at the Stanford University. From 2011 to 2012 he joined Siemens Healthcare as innovation project manager and was responsible for reconstruction topics in the Angiography and X-ray business unit.

In 2012, he returned the University of Erlangen-Nuremberg as head of the Medical Reconstruction Group at the Pattern Recognition lab. In 2015 he became professor and head of the Pattern Recognition Lab. Since 2016, he is member of the steering committee of the European Time Machine Consortium. In 2018, he was awarded an ERC Synergy Grant "4D nanoscope".  Current research interests focuses on medical imaging, image and audio processing, digital humanities, and interpretable machine learning and the use of known operators.

2024

• Digitaler Registerassistent

  (Third Party Funds Single)

  Project leader: Stephanie Evert, Andreas Maier, Lutz Schröder, Axel Adrian, Michael Kohlhase
  Term: March 1, 2024 - February 28, 2027
  Acronym: DIREGA
  Funding source: andere Förderorganisation
  URL: https://www.direga.fau.de
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• Coordinated grid protection based on machine learning methods

  (Third Party Funds Single)

  Project leader: Andreas Maier, Johann Jäger, Siming Bayer
  Term: July 1, 2024 - June 30, 2027
  Acronym: Netzschutz-KI
  Funding source: DFG-Einzelförderung / Sachbeihilfe (EIN-SBH)
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2023

• Artificial Intelligent as a Market Participant – Implications for Antitrust Law

  (FAU Funds)

  Project leader: Siming Bayer
  Term: January 15, 2023 - January 14, 2024
  Abstract

  Introduction: Antitrust laws (also known ascompetition laws) are designed to encourage strong competition and are designedto protect consumers from predatory commercial practices. The primary goals ofantitrust law are to ensure the functioning of the markets and to ensure faircompetition. A prominent example of an antitrust violation is illegal pricefixing. By definition, it is an agreement between competitors that fixes pricesor other competitive conditions, and thus violates the principle of the pricingmechanism through free market forces. A typical feature of illegal price fixingis verifiable communication (written or verbal) between human marketparticipants. However, in the age of artificial intelligence and e-commerce,the definition and the detection of this illegal practice faces new challengesas collusive behaviors that violate antitrust laws, such as the pricingmechanism, can be partially or fully automated [1]. Furthermore, thecommunications between market participants can be both overt and covert. Finally,market participants can be artificial agents which might affected by perverseinstantiation [2]. In other words, new technological possibilities areavailable to disguise illegal pricing policies and business practices.

  Recent research, mainly from theeconomic and jurisprudence point of view, concludes the intensive applicationof AI algorithms in E-commerce will increase the extend of known forms ofanticompetitive behaviors [3][4]. However, the questions regarding whether andto which extent collusive behaviors will emerge by AI itself (which is anunknown form of anticompetitive behaviors) are rarely understood. Feasibilitystudies and comprehensive analysis comprising the implementation of AI methods andvalidation of the derived hypothesis has not been conducted so far. Therefore,the main goals of this project are to investigate the possibilities of collusivebehaviors stimulated and/or emerged by AI algorithms on digital marketplace andderive consequences on the antitrust law as well as competition policies. Tothe best of our knowledge, this is the first time that a research project inthe field of Antitrust and AI (AAI) is focusing on the mathematical andalgorithmic perspective of the question to which extend the utilization of AImethods is facilitating the collusive behaviors in the era of digital economy.

  Objectives: In order to validate the hypothesesthat AI algorithms is able to develop and communicate collusive behaviors ondigital marketplaces both in overt and covert fashion, comprehensive emulatorsof online marketplaces in different setups will be implemented.  Furthermore, different communication channels(both overt and covert) of digital marketplaces will be discovered and understood,as it is highly relevant to the detection of collusive practices. Finally, differentonline trading scenarios utilizing AI algorithms will be established and theimpact on antitrust law and competition polices will be derived. In total, the mainaspects in the intended DFG-application can be summarized as follows:

  1.      Asthe research topic belongs to a highly interdisciplinary field, a comprehensiveliterature review is necessary to define the problem space of the research andis of great importance to conduct the subsequent experiments successfully.Therefore, a comprehensive literature review on the aspects of antitrust law, gametheory, artificial intelligence and cyber security will be conducted.

  2.      Firststep of the implementation is the holistic emulation of the digitalmarketplace. The market emulator should have the capability to emulate the digitalmarket following various rules (e.g., Cournot vs. collusive competition) indifferent size (i.e., with different amount of market participants). Moreover,state-of-the-art algorithms for dynamic pricing should be replicated andintegrated into the market emulator as well.

  3.      Afurther aspect of this project is the communication mechanism in the era of E-commerceand AI. The know form of collusions mostly utilize overt communications.However, covert communication channels (i.e., communication channels that are notoriginally designed for the communication purpose, therefore hardly to bedetected [5][6]) poses further vulnerabilities of online marketplaces. The mechanismsand capacities of covert channels facilitating the collusive behaviors (e.g.,illegal price fixing) as should be investigated with the implemented marketemulator.

  4.      Finally,artificial agents for price definition of different products should be proposedand implemented following different competition models as well as marketcomplexities, aiming at understanding the central research questions of thisresearch project, i.e., capabilities and conditions of emerging collusivebehaviors of artificial agents by themselves. This particular step can beachieved by using reinforcement learning techniques. Technical opportunitiesand challenges for the discrimination of collusive and non-collusive behaviorsthat are potentially emerged by the artificial agents should be explored aswell.

  The entire project will besupervised by experts from three disciplines. Prof. Jochen Hoffmann (chair of Private Business Law) will support this research project with his knowledges and expertiseon antitrust law, Prof. Felix Feilling (chair of Cyber Security) will advise onthe aspects that are related to covert communication and cyber security, andProf. Andreas Maier (pattern recognition lab) will mentor this project from theAI point of view.

  [1] KünstlicheIntelligenz als Marktteilnehmer – Technische Möglichkeiten, Maier A., Bayer S.,Mohr Verlag. Submitted, unpublished.

  [2] BostromN. Superintelligence: Paths, Dangers, Strategies. Minds & Machines 25, Seite 285–289 (2015).

  [3] Petit, N. Antitrust andartificial intelligence: A research agenda. In: Journal of European CompetitionLaw and Practice. Vol. 8, Issue 6, pp. 361–362. Oxford University Press.(2017)

  [4] Beneke, F., Mackenrodt, M.,Remedies for algorithmic tacit collusion, Journal of Antitrust Enforcement,Volume 9, Issue 1, Pages 152–176 (2021).

  [5]Hans-Georg Eßer, Felix C. Freiling. Kapazitätsmessung eines verdecktenZeitkanals über HTTP, Univ. Mannheim,Technischer Bericht TR-2005-10, November 2005. (2005)

  [6] Freiling F.C., Schinzel S.Detecting Hidden Storage Side Channel Vulnerabilities in NetworkedApplications. In: Camenisch J., Fischer-Hübner S., Murayama Y., Portmann A.,Rieder C. (eds) Future Challenges in Security and Privacy for Academia andIndustry. SEC 2011. IFIP Advances in Information and Communication Technology,vol 354. Springer, Berlin, Heidelberg. (2011)

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• An AI-based framework for visualizing and analyzing massive amounts of 4D tomography data for beamline end users

  (Third Party Funds Group – Overall project)

  Project leader: Andreas Maier, Yipeng Sun
  Term: March 1, 2023 - February 28, 2026
  Acronym: KI4D4E
  Funding source: Bundesministerium für Forschung, Technologie und Raumfahrt (BMFTR)
  URL: https://foerderportal.bund.de/foekat/jsp/SucheAction.do?actionMode=view&fkz=05D23WE1
  Abstract

  Synchrotron tomography is characterized by extremely brilliant X-rays, which enables almost artifact-free imaging. Furthermore, very high resolution can be achieved by using special X-ray optics, and the special design of synchrotron facilities also allows fast in-situ experiments, i.e. 4D tomography.  The combination of these features enables high-resolution computed tomography on objects where conventional laboratory CT fails. At the same time, however, this also produces enormous amounts of data that are generally unprocessable by end users, pushing even the operators of synchrotrons to their limits.

  The goal of the KI4D4E project is to develop AI-based methods that can be used by end users to process the enormous amounts of data in such 4D CT measurements. This includes improving image quality through artifact reduction, reduction and accessibility of data to end users to help the latter interpret the results.

  The project focuses on the topics of artifact reduction, segmentation and visualization of large 4D data sets. The resulting methods should be applicable to data from both photon and neutron sources.

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• Exploring Brain Mechanics (EBM): Understanding, engineering and exploiting mechanical properties and signals in central nervous system development, physiology and pathology

  (Third Party Funds Group – Overall project)

  Project leader: Paul Steinmann
  Term: January 1, 2023 - December 31, 2026
  Acronym: SFB 1540 - EBM
  Funding source: DFG / Sonderforschungsbereich / Transregio (SFB / TRR)
  URL: https://www.crc1540-ebm.research.fau.eu/
  Abstract

  Thecentral nervous system (CNS) is our most complex organ system. Despite tremendousprogress in our understanding of the biochemical, electrical, and geneticregulation of CNS functioning and malfunctioning, many fundamental processesand diseases are still not fully understood. For example, axon growth patterns inthe developing brain can currently not be well-predicted based solely on thechemical landscape that neurons encounter, several CNS-related diseases cannotbe precisely diagnosed in living patients, and neuronal regeneration can stillnot be promoted after spinal cord injuries.

  Duringmany developmental and pathological processes, neurons and glial cells aremotile. Fundamentally, motion is drivenby forces. Hence, CNS cells mechanicallyinteract with their surrounding tissue. They adhere to neighbouring cells and extracellular matrix using celladhesion molecules, which provide friction, and generate forces usingcytoskeletal proteins.  These forces aretransmitted to the outside world not only to locomote but also to probe themechanical properties of the environment, which has a long overseen huge impacton cell function.

  Onlyrecently, groups of several project leaders in this consortium, and a few other groupsworldwide, have discovered an important contribution of mechanical signalsto regulating CNS cell function. For example, they showed that brain tissuemechanics instructs axon growth and pathfinding in vivo, that mechanicalforces play an important role for cortical folding in the developing humanbrain, that the lack of remyelination in the aged brain is due to an increasein brain stiffness in vivo, and that many neurodegenerative diseases areaccompanied by changes in brain and spinal cord mechanics. These first insights strongly suggest thatmechanics contributes to many other aspects of CNS functioning, and it islikely that chemical and mechanical signals intensely interact at the cellularand tissue levels to regulate many diverse cellular processes.

  The CRC 1540 EBM synergises the expertise of engineers, physicists,biologists, medical researchers, and clinicians in Erlangen to explore mechanicsas an important yet missing puzzle stone in our understanding of CNSdevelopment, homeostasis, and pathology. Our strongly multidisciplinary teamwith unique expertise in CNS mechanics integrates advanced invivo, in vitro, and in silico techniques across time(development, ageing, injury/disease) and length (cell, tissue, organ) scalesto uncover how mechanical forces and mechanical cell and tissue properties,such as stiffness and viscosity, affect CNS function. We especially focus on(A) cerebral, (B) spinal, and (C) cellular mechanics. Invivo and in vitro studies provide a basic understanding ofmechanics-regulated biological and biomedical processes in different regions ofthe CNS. In addition, they help identify key mechano-chemical factors forinclusion in in silico models and provide data for model calibration andvalidation. In silico models, in turn, allow us to test hypotheses without the need of excessive or even inaccessibleexperiments. In addition, they enable the transfer and comparison of mechanics data and findingsacross species and scales. They also empower us to optimise processparameters for the development of in vitro brain tissue-like matricesand in vivo manipulation of mechanical signals, and, eventually, pavethe way for personalised clinical predictions.

  Insummary, we exploit mechanics-based approaches to advance ourunderstanding of CNS function and to provide the foundation for futureimprovement of diagnosis and treatment of neurological disorders.

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• AI-refined thermo-hydraulic model for the improvement of the efficiency and quality of water supply

  (Third Party Funds Single)

  Project leader: Siming Bayer, Andreas Maier
  Term: November 1, 2023 - October 31, 2026
  Acronym: OptiHyd
  Funding source: Bayerisches Staatsministerium für Wirtschaft, Landesentwicklung und Energie (StMWi) (seit 2018)
  Abstract

  The United Nations' goals for sustainable development have made improving quality of life and access to clean drinking water a political priority. However, in recent decades, the water cycle in Bavaria has also been significantly affected by climate change. Two important aspects of daily drinking water supply and distribution are the assurance of water quality and the increase in usage efficiency. To enhance the resilience and capacity of the water supply in general, numerical simulation, data integration, and artificial intelligence (AI) are necessary. In this project, we aim to develop an AI-refined temperature-hydraulic model using heterogeneous data sources from a Bavarian water supply network. Hybrid AI methods are employed to model the complex relationship between water and soil temperature. The resulting model will serve as the basis for various real applications such as leak detection, anomaly recognition, and monitoring of drinking water quality, with the overarching goal of increasing the efficiency and quality of the water supply while simultaneously contributing to the containment of the impact of climate change on drinking water supply

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• Maschinelles Lernen und Datenanalyse für heterogene, artübergreifende Daten (X02)

  (Third Party Funds Group – Sub project)

  Overall project: SFB 1540: Erforschung der Mechanik des Gehirns (EBM): Verständnis, Engineering und Nutzung mechanischer Eigenschaften und Signale in der Entwicklung, Physiologie und Pathologie des zentralen Nervensystems
  Project leader: Katharina Breininger, Andreas Maier
  Term: January 1, 2023 - December 31, 2026
  Acronym: SFB 1540 X02
  Funding source: DFG / Sonderforschungsbereich (SFB)
  Abstract

  X02 nutzt die in EBM erzeugten Bilddaten und mechanischen Messungen, um Deep Learning-Methoden zu entwickeln, die Wissen über Spezies hinweg transferieren. In silico und in vitro Analysen werden deutlich spezifischere Daten liefern als in vivo Experimente, insbesondere für menschliches Gewebe. Um hier Erkenntnisse aus datenreichen Experimenten zu nutzen, werden wir Transfer Learning-Algorithmen für heterogene Daten entwickeln. So kann maschinelles Lernen auch unter stark datenlimitierten Bedingungen nutzbar gemacht werden. Ziel ist es, ein holistisches Verständnis von Bilddaten und mechanischen Messungen über Artgrenzen hinweg zu ermöglichen.

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2022

• International Doctoral Program: Measuring and Modelling Mountain glaciers and ice caps in a Changing Climate (M³OCCA)

  (Third Party Funds Single)

  Project leader: Matthias Braun
  Term: June 1, 2022 - May 31, 2026
  Acronym: MOCCA
  Funding source: Elitenetzwerk Bayern
  Abstract

  Mountain glaciers and ice caps outside the large ice sheets of Greenland and Antarctica contribute about 41% to the global sea level rise between 1901 to 2018 (IPCC 2021). While the Arctic ice masses are and will remain the main contributors to sea level rise, glacier ice in other mountain regions can be critical for water supply (e.g. irrigation, energy generation, drinking water, but also river transport during dry periods). Furthermore, retreating glaciers also can cause risks and hazards by floods, landslides and rock falls in recently ice-free areas. As a consequence, the Intergovernmental Panel of Climate Change (IPCC) dedicates special attention to the cryosphere (IPCC 2019; IPCC 2021). WMO and UN have defined Essential Climate Variables (ECV) for assessing the status of the cryosphere and its changes. These ECVs should be measured regularly on large scale and are essential to constrain subsequent modelling efforts and predictions.
  The proposed International Doctorate Program (IDP) “Measuring and Modelling Mountain glaciers and ice caps in a Changing ClimAte (M3OCCA)” will substantially contribute to improving our observation and measurement capabilities by creating a unique inter- and transdisciplinary research platform. We will address main uncertainties of current measurements of the cryosphere by developing new instruments and future analysis techniques as well as by considerably advancing geophysical models in glaciology and natural hazard research. The IDP will have a strong component of evolving techniques in the field of deep learning and artificial intelligence (AI) as the data flow from Earth Observation (EO) into modelling increases exponentially. IDP M3OCCA will become the primary focal point for mountain glacier research in Germany and educate emerging
  talents with an interdisciplinary vision as well as excellent technical and soft skills. Within the IDP we combine cutting edge technologies with climate research. We will develop future technologies and transfer knowledge from other disciplines into climate and glacier research to place Bavaria at the forefront in the field of mountain cryosphere research. IDP M3OCCA fully fits into FAU strategic goals and it will leverage on Bavaria’s existing long-term commitment via the super test site Vernagtferner in the Ötztal Alps run by Bavarian Academy of Sciences (BAdW). In addition, we cooperate with the University of Innsbruck and its long-term observatory at Hintereisferner. At those super test sites, we will perform joint measurements, equipment tests, flight campaigns and cross-disciplinary trainings and exercises for our doctoral researchers. We leverage on existing
  instrumentation, measurements and time series. Each of the nine doctoral candidates will be guided by interdisciplinary, international teams comprising university professors, senior scientists and emerging talents from the participating universities and external research organisations.

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• Temporally resolved 3-D retinal blood flow quantification using advanced motion correction and signal reconstruction in optical coherence tomography angiography

  (Third Party Funds Single)

  Project leader: Stefan Ploner, Andreas Maier
  Term: since November 15, 2022
  Acronym: 4D-OCTA
  Funding source: DFG-Einzelförderung / Sachbeihilfe (EIN-SBH)
  Abstract

  Die optische Kohärenztomographie (OCT) erzeugt volumetrische 3-D-Bilder von Gewebe mit Mikrometerauflösung, indem sie einen Laserstrahl zum Scannen verwendet und die Amplitude und Zeitverzögerung von zurückgestreutem Licht misst. Die OCT hat einen großen Einfluss auf die Augenheilkunde und wurde zu einer Standard-Bildgebungsmodalität für die Diagnose, die Überwachung des Krankheitsverlaufs und das Ansprechen auf die Behandlung sowie für die Untersuchung der Pathogenese von Krankheiten wie diabetischer Retinopathie, altersbedingter Makuladegeneration und Glaukom. Die jüngste Entwicklung der OCT-Angiographie (OCTA) hat die grundlegende und klinische Forschung dramatisch beschleunigt. OCTA führt eine tiefenaufgelöste (3-D) Bildgebung der retinalen Mikrovaskulatur durch, indem es wiederholt die gleiche Netzhautposition abbildet und den Bewegungskontrast von sich bewegenden Blutzellen erkennt. Im Vergleich zu herkömmlichen Ansätzen, die auf injizierten Kontrastmitteln basieren, hat OCTA den Vorteil, dass es nicht invasiv ist, sodass die Bildgebung bei jedem Patientenbesuch durchgeführt werden kann, was Längsschnittstudien ermöglicht. Allerdings hat OCTA auch einige Einschränkungen. Da eine wiederholte Bildgebung erforderlich ist, um den Blutfluss zu erkennen, sind die Aufnahmezeiten lang und die Daten können durch Augenbewegungen und Bildartefakte verzerrt werden, was eine quantitative Längsschnittanalyse erschwert. OCTA-Algorithmen können das Vorhandensein eines Blutflusses erkennen, sind jedoch nur begrenzt in der Lage, subtile Veränderungen des Flusses aufzulösen, die frühe Anzeichen einer Krankheit sein können. Zeitliche Schwankungen des Flusses, die durch den Herzzyklus oder die funktionelle Reaktion der Netzhaut verursacht werden, sind schwer zu untersuchen. Wir schlagen vor, ein neues Framework für OCTA zu entwickeln, das eine Bewegungskorrektur auf Kapillarebene ermöglicht, Blutflussgeschwindigkeiten differenziert und eine Analyse auf mehreren Zeitskalen ermöglicht (4-D OCTA). Die Fähigkeit, über die Visualisierung der Mikrovaskulatur hinauszugehen und den Fluss und seine zeitlichen Schwankungen zu beurteilen, ermöglicht die Beurteilung subtiler Beeinträchtigungen der mikrovaskulären Perfusion sowie des Herzzyklus und der Reaktion auf funktionelle Stimulation. In Kombination mit der vaskulären strukturellen Bildgebung versprechen diese Fortschritte, neue Krankheitsmarker in früheren Krankheitsstadien bereitzustellen, eine genauere Messung des Krankheitsverlaufs und des Ansprechens auf die Therapie in pharmazeutischen Studien zu ermöglichen und zur Aufklärung der Pathogenese bei Netzhauterkrankungen beizutragen.

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2021

• ODEUROPA: Negotiating Olfactory and Sensory Experiences in Cultural Heritage Practice and Research

  (Third Party Funds Group – Sub project)

  Overall project: ODEUROPA
  Project leader: Peter Bell, Andrea Büttner, Andreas Maier
  Term: January 1, 2021 - December 31, 2022
  Acronym: ODEUROPA
  Funding source: EU - 8. Rahmenprogramm - Horizon 2020
  URL: https://odeuropa.eu/
  Abstract

  Our senses are gateways to the past. Although museums are slowly discovering the power of multi-sensory presentations, we lack the scientific standards, tools and data to identify, consolidate, and promote the wide-ranging role of scents and smelling in our cultural heritage. In recent years, European cultural heritage institutions have invested heavily in large-scale digitization. A wealth of object, text and image data that can be analysed using computer science techniques now exists. However, the potential olfactory descriptions, experiences, and memories that they contain remain unexplored. We recognize this as both a challenge and an opportunity. Odeuropa will apply state-of-the-art AI techniques to text and image datasets that span four centuries of European history. It will identify the vocabularies, spaces, events, practices, and emotions associated with smells and smelling. The project will curate this multi-modal information, following semantic web standards, and store the enriched data in a ‘European Olfactory Knowledge Graph’ (EOKG). We will use this data to identify ‘storylines’, informed by cultural history and heritage research, and share these with different audiences in different formats: through demonstrators, an online catalogue, toolkits and training documentation describing best-practices in olfactory museology. New, evidence-based methodologies will quantify the impact of multisensory visitor engagement. This data will support the implementation of policy recommendations for recognising, promoting, presenting and digitally preserving olfactory heritage. These activities will realize Odeuropa’s main goal: to show that smells and smelling are important and viable means for consolidating and promoting Europe’s tangible and intangible cultural heritage.

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• SmartCT - Erforschung und Entwicklung von Methoden der Künstlichen Intelligenz für ein autonomes Roboter-CT System zur 3D-Digitalisierung beliebiger Objekte

  (Third Party Funds Group – Overall project)

  Project leader: Andreas Maier, Linda-Sophie Schneider
  Term: June 1, 2021 - May 31, 2024
  Acronym: SmartCT
  Funding source: Bayerisches Staatsministerium für Wirtschaft, Landesentwicklung und Energie (StMWi) (seit 2018)
  URL: https://www.pinterguss.de/forschung-entwicklung/smart-ct.html
  Abstract

  In Vorhaben SmartCT sollen KI-Methoden entwickelt und angewendet werden, die Roboter-CT Systemen ermöglicht, selbstständig, also autonom, die äußeren und inneren Strukturen beliebiger Objekte zu digitalisieren. Diese so erzeugten Daten stellen die Basis von neuartigen, innovativen und datengetriebenen Geschäftsmodellen in vielen Bereichen wie Produktentwicklung, Produktion, Handel, Instandhaltung, Sicherheit und Recycling dar.
  Roboter-CT Systeme können beliebige Objekte (Fahrzeugkomponenten, Flugzeugflügel, Batterie-zellen, Versandpaket, etc.) zerstörungsfrei digitalisieren. Diese Systeme sind jedoch hoch komplex und deshalb bisher nur mit großem zeitlichen Aufwand von Experten bedien- und einsetzbar. Roboter-CT Systeme werden deshalb aktuell nur bei großen Unternehmen eingesetzt. Mit Hilfe der in SmartCT entwickelten KI-Methoden soll es möglich werden, dass beliebige Objekte effizient und wirtschaftlich attraktiv digitalisiert werden können, so dass auch kleinere und mittlere Unternehmen die Vorteile dieser Technologie vollständig zugänglich gemacht werden kann. Zugleich wird mit diesem Vorhaben die Akzeptanz roboterbasierter CT-Systeme in der Industrie nachhaltig erhöht.

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• UtilityTwin

  (Third Party Funds Group – Overall project)

  Project leader: Andreas Maier, Siming Bayer, Adithya Ramachandran
  Term: September 1, 2021 - August 31, 2024
  Acronym: UtilityTwin
  Funding source: Bayerisches Staatsministerium für Wirtschaft, Landesentwicklung und Energie (StMWi) (seit 2018)
  Abstract

  In the UtilityTwin research project, an intelligent digital twin for any energy or water supply network is to be researched and developed on the basis of adaptive high-resolution sensor data (down to the sub-second range) and machine learning techniques. Overall, the technology concepts BigData and AI are to be combined in an innovative way in this research project in order to make positive contributions to the implementation of the energy transition and to counteract climate change.

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2020

• Bereitstellung einer Infrastruktur zur Nutzung für die Ausbildung Studierender auf einem z/OS Betriebssystem der Fa. IBM

  (FAU Funds)

  Project leader: Andreas Maier
  Term: April 2, 2020 - March 31, 2025
  Acronym: Betriebssystem IBM
  Funding source: Friedrich-Alexander-Universität Erlangen-Nürnberg
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• Automatic exposure control (AEC) for CT based on neural network-driven patient-specific real-time assessment of dose distributions and minimization of the effective dose

  (Third Party Funds Single)

  Project leader: Andreas Maier
  Term: April 1, 2020 - March 31, 2023
  Funding source: DFG-Einzelförderung / Sachbeihilfe (EIN-SBH)
  Abstract

  Modern diagnostic CT systems comprise a variety of measures to keep patient dose at a minimum. Of particular importance is the tube current modulation (TCM) technique that automatically adapts the tube current for each projection in a way to minimize the tube current time product (mAs-product) for a given image quality. This can also be regarded as maximizing the image quality for a given mAs-product. TCM performs a modulation depending on the angular position of the x-ray tube and depending on the z-position of the scan. Measures related to TCM are the automated choice of the mean tube current and of the optimal tube voltage. These three dose reduction methods are also known under the term automatic exposure control (AEC).As of today, however, the AEC does not minimize the actual patient dose and thereby the actual patient risk. It rather minimizes surrogates thereof. The surrogate of TCM is the mAs-product. The surrogate used to automatically select the tube voltage is the CTDI value or the dose length product (DLP). A direct minimization of the weighted summed organ dose values and thereby the patient risk is currently not practicable due to a) the very high computation times of the Monte Carlo dose calculation algorithms and b) due to the lack of a reliable segmentation of the radiation sensitive and risk-relevant organs.We therefore plan to use artificial neural networks to solve the above-mentioned problems and to realize a new AEC which is capable of directly minimizing patient dose and risk instead of using surrogate parameters. A first neural net will convert the patient topogram(s) into a coarse estimate of the CT volume. In cases where only a single topogram is available information of the table height will be used for this estimation. A second neural net will segment the relevant organs. We can here partially use prior work of a previous DFG project (KA 1678/20, LE 2763/2, MA 4898/5). A third network will use further scan parameters (table increment, pitch value, rotation time, collimation, tube voltage, …) to compute the expected dose distribution per projection. This, together with the segmentation of the organs, shall be used to compute the effective dose (or risk) or the patient per projection. A minimization algorithm will then find the optimal tube current curve that minimizes patient risk at a given image quality or that maximizes image quality at a given patient risk.To evaluate our deep AEC algorithm diagnostic CT data will be collected. The data will be retrospectively converted to the desired tube current curve by adding noise to the rawdata followed by another reconstruction. Experienced radiologists will then perform a blinded study where they read images produced without AEC, with the conventional AEC as of today, and with our new deep AEC algorithm.
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• Entwicklung eines Leitfadens zur dreidimensionalen zerstörungsfreien Erfassung von Manuskripten

  (Third Party Funds Single)

  Project leader: Jan Schür
  Term: since November 1, 2020
  Funding source: DFG-Einzelförderung / Sachbeihilfe (EIN-SBH)
  URL: https://gepris.dfg.de/gepris/projekt/433501541
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• Förderantrag zur Entwicklung des Kurses „Deep Learning for beginners“

  (Third Party Funds Single)

  Project leader: Andreas Maier
  Term: September 1, 2020 - August 31, 2021
  Funding source: Virtuelle Hochschule Bayern
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• Integratives Konzept zur personalisierten Präzisionsmedizin in Prävention, Früh-Erkennung, Therapie und Rückfallvermeidung am Beispiel von Brustkrebs

  (Third Party Funds Single)

  Project leader: Matthias Beckmann, Peter Fasching, Björn Eskofier, Peter Dabrock, Hans-Ulrich Prokosch, Andreas Maier, Oliver Schöffski
  Term: October 1, 2020 - September 30, 2024
  Acronym: DigiOnko FAU
  Funding source: Bayerisches Staatsministerium für Gesundheit und Pflege, StMGP (seit 2018)
  Abstract

  Breast cancer is one of the leading causes of death in the field of oncology in Germany. For the successful care and treatment of patients with breast cancer, a high level of information for those affected is essential in order to achieve a high level of compliance with the established structures and therapies. On the one hand, the digitalisation of medicine offers the opportunity to develop new technologies that increase the efficiency of medical care. On the other hand, it can also strengthen patient compliance by improving information and patient integration through electronic health applications. Thus, a reduction in mortality and an improvement in quality of life can be achieved. Within the framework of this project, digital health programmes are going to be created that support and complement health care. The project aims to provide better and faster access to new diagnostic and therapeutic procedures in mainstream oncology care, to implement eHealth models for more efficient and effective cancer care, and to improve capacity for patients in oncologcal therapy in times of crisis (such as the SARS-CoV-2 pandemic). The Chair of Health Management is conducting the health economic evaluation and analysing the extent to which digitalisation can contribute to a reduction in the costs of treatment and care as well as to an improvement in the quality of life of breast cancer patients.

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• Integratives Konzept zur personalisierten Präzisionsmedizin in Prävention, Früh-Erkennung, Therapie undRückfallvermeidung am Beispiel von Brustkrebs - DigiOnko

  (Third Party Funds Single)

  Project leader: Matthias Beckmann, Björn Eskofier, Peter Dabrock, Hans-Ulrich Prokosch, Andreas Maier, Oliver Schöffski
  Term: October 1, 2020 - September 30, 2024
  Acronym: DigiOnko UKER
  Funding source: Bayerisches Staatsministerium für Gesundheit und Pflege, StMGP (seit 2018)
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• Intelligente MR-Diagnostik der Leber durch Verknüpfung modell- und datengetriebener Verfahren

  (Third Party Funds Single)

  Project leader: Andreas Maier
  Term: April 1, 2020 - March 31, 2023
  Acronym: iDeLIVER
  Funding source: Bundesministerium für Forschung, Technologie und Raumfahrt (BMFTR)
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• Intelligent MR Diagnosis of the Liver by Linking Model and Data-driven Processes (iDELIVER)

  (Third Party Funds Single)

  Project leader: Andreas Maier, Zijin Yang
  Term: August 3, 2020 - March 31, 2023
  Funding source: Bundesministerium für Forschung, Technologie und Raumfahrt (BMFTR)
  Abstract

  The project examines the use and further development of machine learning methods for MR image reconstruction and for the classification of liver lesions. Based on a comparison model and data-driven image reconstruction methods, these are to be systematically linked in order to enable high acceleration without sacrificing diagnostic value. In addition to the design of suitable networks, research should also be carried out to determine whether metadata (e.g. age of the patient) can be incorporated into the reconstruction. Furthermore, suitable classification algorithms on an image basis are to be developed and the potential of direct classification on the raw data is to be explored. In the long term, intelligent MR diagnostics can significantly increase the efficiency of use of MR hardware, guarantee better patient care and set new impulses in medical technology.

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• Molecular Assessment of Signatures ChAracterizing the Remission of Arthritis

  (Third Party Funds Single)

  Project leader: Georg Schett, Uwe Sonnewald, Andreas Maier
  Term: April 1, 2020 - September 30, 2022
  Acronym: MASCARA
  Funding source: Bundesministerium für Forschung, Technologie und Raumfahrt (BMFTR)
  Abstract

  MASCARA zielt auf eine detaillierte, molekulare Charakterisierung der Remission bei Arthritis ab. Das Projekt basiert auf der kombinierten klinischen und technischen Erfahrung von Rheumatologen, Radiologen, Medizinphysikern, Nuklearmedizinern, Gastroenterologen, grundlagenwissenschaftlichen Biologen und Informatikern und verbindet fünf akademische Fachzentren in Deutschland. Das Projekt adressiert 1) den Umstand der zunehmenden Zahl von Arthritis Patienten in Remission, 2) die Herausforderungen, eine effektive Unterdrückung der Entzündung von einer Heilung zu unterscheiden und 3) das begrenzte Wissen über die Gewebeveränderungen in den Gelenken von Patienten mit Arthritis. MASCARA wird auf der Grundlage vorläufiger Daten vier wichtige mechanistische Bereiche (immunstoffwechselbedingte Veränderungen, mesenchymale Gewebereaktionen, residente Immunzellen und Schutzfunktion des Darms) untersuchen, die gemeinsam den molekularen Zustand der Remission bestimmen. Das Projekt zielt auf die Sammlung von Synovialbiopsien und die anschließende Gewebeanalyse bei Patienten mit aktiver Arthritis und Patienten in Remission ab. Die Gewebeanalysen umfassen (Einzelzell)-mRNA-Sequenzierung, Massenzytometrie sowie die Messung von Immunmetaboliten und werden durch molekulare Bildgebungsverfahren wie CEST-MRT und FAPI-PET ergänzt. Sämtliche Daten, die in dem Vorhaben generiert werden, werden in einem bereits bestehenden Datenbanksystem mit den Daten der anderen Partner zusammengeführt und gespeichert. Das Zusammenführen der Daten soll – mit Hilfe von maschinellem Lernen – krankheitsspezifische und mit der Krankheitsaktivität verbundene Mustermatrizen identifizieren.

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• Entwicklung eines Leitfadens zur dreidimensionalen zerstörungsfreien Erfassung von Manuskripten

  (Third Party Funds Single)

  Project leader: Tino Hausotte, Jan Schür, Andreas Maier, Gisela Anton
  Term: May 1, 2020 - April 30, 2022
  Funding source: DFG-Einzelförderung / Sachbeihilfe (EIN-SBH)
  URL: https://gepris.dfg.de/gepris/projekt/433501541?context=projekt&task=showDetail&id=433501541&
  Abstract

  In the course of massive digitization, a large part of libraries’ archived documents are currently being converted into electronic formats. However, the digitization is also reaching its limits. Scanning robots cannot digitize documents whose condition due to natural ageing or external influences prohibit a conventional, optical based processing. Our own preliminary work has shown that the three imaging techniques X-ray Computed Tomography, Phase Contrast X-ray Computed Tomography and Terahertz Imaging are suitable for providing non-invasive insights into such documents, allow the acquisition of digital imaging information and are capable to re-enable an efficient automated process to digitalize cultural heritage documents.This research project is the first to develop a concrete digitization strategy or method for such documents. This structured evaluation will be based on a quality value that allows statements to be made about the expected result of digitization with one of the mentioned modalities for certain historical materials. From this, the most suitable imaging procedure can be determined. Based on these findings, a guideline for the digitization of fragile documents will be developed to predict the quality, feasibility and possible damage before a scan. In addition, algorithms will be developed that virtually process the generated data and make it readable for the human eye. Three concrete goals will be pursued to carry out the research project. By evaluating the modalities for selected historical materials, the most appropriate procedure for a specific document should then be identified. At the end of the project, a guide will be made available and the possibilities of each modality will be demonstrated by specifying material combinations and relevant parameters. It will be possible to test the variation of the recording parameters and to display exemplary results using the generated database. This also makes it possible to calculate a quality value. The basis for such a guide is the evaluation of the three modalities for relevant materials. For this purpose, realistic test specimen are produced. Both the scan quality and resolution as well as possible damage to the document must be considered. The guide will then be used to identify the most suitable procedure for a specific document. This statement is based on the mentioned quality value, which will also be used to predict the optimal digitization modality and the quality for an unknown document.The evaluation of several modalities as well as the development of algorithms are to be seen as central challenges of the research project. It will be possible to store endangered holdings in a digital format without destroying their structure through manual intervention. In the second funding phase, a multi-modal solution should be investigated in which disadvantages and limitations of individual modalities will be compensated by combining several modalities.
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• Verbesserte Dual Energy Bildgebung mittels Maschinellem Lernen

  (Third Party Funds Single)

  Project leader: Andreas Maier
  Term: April 1, 2020 - December 31, 2020
  Funding source: Europäische Union (EU)
  Abstract

  The project aims to develop novel and innovative methods to improve visualisation and use of dual energy CT (DECT) images. Compared to conventional single energy CT (SECT) scans, DECT contains a significant amount of additional quantitative information that enables tissue characterization far beyond what is possible with SECT, including material decomposition for quantification and labelling of specific materials within tissues, creation of reconstructions at different predicted energy levels, and quantitative spectral tissue characterization for tissue analysis. However, despite the many potential advantages of DECT, applications remain limited and in specizlized clinical settings. Some reasons are that many applications are specific for the organ under investigation, require additional, manual processing or calibration, and not easily manipulated using standard interactive contrast visualisation windows available in clinical viewing stations. This is a significant disadvantage compared to conventional SECT.
  In this project, we propose to develop new strategies to fuse and display the additional DECT information on a single contrast scale such that it can be visualised with the same interactive tools that radiologists are used to in their clinical routine. We will investigate non-linear manifold learning techniques like Laplacian Eigenmaps and the Sammon Mapping. Both allow extension using AI-based techniques like the newly developed user loss that allows to integrate user's opinions using forced choice experiments. This will allow a novel image contrast that will be compatible with interactive window and level functions that are rourintely used by radiologists. Furthermore, we aim at additional developments that will use deep neural networks to approximate the non-linear mapping function and to generate reconstructions that capture and display tissue specific spectral characteristics in a readily and universally useable manner for enhancing diagnostic value.

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2019

• ICONOGRAPHICS: Computational Understanding of Iconography and Narration in Visual Cultural Heritage

  (FAU Funds)

  Project leader: Peter Bell, Andreas Maier, Corinna Reinhardt, Ute Verstegen
  Term: April 1, 2019 - March 31, 2021
  Acronym: ICONOGRAPHICS
  Abstract

  The interdisciplinary research project Iconographics is dedicated to innovative possibilities of digital image recognition for the arts and humanities. While computer vision is already often able to identify individual objects or specific artistic styles in images, the project is confronted with the open problem of also opening up the more complex image structures and contexts digitally. On the basis of a close interdisciplinary collaboration between Classical Archaeology, Christian Archaeology, Art History and the Computer Sciences, as well as joint theoretical and methodological reflection, a large number of multi-layered visual works will be analyzed, compared and contextualized. The aim is to make the complex compositional, narrative and semantic structures of these images tangible for computer vision.

  Iconography and Narratology are identified as a challenging research questions for all subjects of the project. The iconography will be interpreted in its plot, temporality, and narrative logic. Due to its complex cultural structure; we selected four important scenes:

  1. The Annunciation of the Lord
  2. The Adoration of the Magi
  3. The Baptism of Christ
  4. Noli me tangere (Do not touch me)
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• Improving multi-modal quantitative SPECT with Deep Learning approaches to optimize image reconstruction and extraction of medical information

  (Non-FAU Project)

  Project leader: Maximilian Reymann
  Term: April 1, 2019 - April 30, 2022
  Acronym: IMQSDL
  Abstract

  This project aims to improve multi-modal quantitative SPECT with Deep Learning approaches to optimize image reconstruction and extraction of medical information. Such improvements include noise reduction and artifact removal from data acquired in SPECT.

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• Advancing osteoporosis medicine by observing bone microstructure and remodelling using a four-dimensional nanoscope

  (Third Party Funds Single)

  Project leader: Georg Schett, Andreas Maier
  Term: April 1, 2019 - March 31, 2025
  Acronym: 4-D nanoSCOPE
  Funding source: European Research Council (ERC)
  URL: https://cordis.europa.eu/project/id/810316
  Abstract

  Due to Europe's ageing society, there has been a dramatic increase in the occurrence of osteoporosis (OP) and related diseases. Sufferers have an impaired quality of life, and there is a considerable cost to society associated with the consequent loss of productivity and injuries. The current understanding of this disease needs to be revolutionized, but study has been hampered by a lack of means to properly characterize bone structure, remodeling dynamics and vascular activity. This project, 4D nanoSCOPE, will develop tools and techniques to permit time-resolved imaging and characterization of bone in three spatial dimensions (both in vitro and in vivo), thereby permitting monitoring of bone remodeling and revolutionizing the understanding of bone morphology and its function.

  To advance the field, in vivo high-resolution studies of living bone are essential, but existing techniques are not capable of this. By combining state-of-the art image processing software with innovative 'precision learning' software methods to compensate for artefacts (due e.g. to the subject breathing or twitching), and innovative X-ray microscope hardware which together will greatly speed up image acquisition (aim is a factor of 100), the project will enable in vivo X-ray microscopy studies of small animals (mice) for the first time. The time series of three-dimensional X-ray images will be complemented by correlative microscopy and spectroscopy techniques (with new software) to thoroughly characterize (serial) bone sections ex vivo.

  The resulting three-dimensional datasets combining structure, chemical composition, transport velocities and local strength will be used by the PIs and international collaborators to study the dynamics of bone microstructure. This will be the first time that this has been possible in living creatures, enabling an assessment of the effects on bone of age, hormones, inflammation and treatment.

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• Advancing osteoporosis medicine by observing bone microstructure and remodelling using a fourdimensional nanoscope

  (Third Party Funds Group – Sub project)

  Overall project: Advancing osteoporosis medicine by observing bone microstructure and remodelling using a fourdimensional nanoscope
  Project leader: Andreas Maier
  Term: April 1, 2019 - March 31, 2025
  Acronym: 4-D nanoSCOPE
  Funding source: EU - 8. Rahmenprogramm - Horizon 2020
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• Artificial Intelligence for Reinventing European Healthcare

  (Third Party Funds Group – Sub project)

  Overall project: Artificial Intelligence for Reinventing European Healthcare
  Project leader: Andreas Maier
  Term: January 1, 2019 - December 31, 2019
  Acronym: ai4euhealth
  Funding source: EU - 8. Rahmenprogramm - Horizon 2020
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• Big Data of the Past for the Future of Europe

  (Third Party Funds Group – Sub project)

  Overall project: TIME MACHINE : BIG DATA OF THE PAST FOR THE FUTURE OF EUROPE
  Project leader: Andreas Maier
  Term: March 1, 2019 - February 29, 2020
  Acronym: Time Machine
  Funding source: EU - 8. Rahmenprogramm - Horizon 2020
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• Deep-Learning basierte Segmentierung und Landmarkendetektion auf Röntgenbildern für unfallchirurgische Eingriffe

  (Third Party Funds Single)

  Project leader: Andreas Maier, Florian Kordon
  Term: since May 6, 2019
  Funding source: Siemens AG
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• Kombinierte Iterative Rekonstruktion und Bewegungskompensation für die Optische Kohärenz Tomographie-Angiographie

  (Third Party Funds Single)

  Project leader: Andreas Maier
  Term: June 1, 2019 - May 31, 2021
  Funding source: DFG-Einzelförderung / Sachbeihilfe (EIN-SBH)
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• Kommunikation und Sprache im Reich. Die Nürnberger Briefbücher im 15. Jahrhunddert: Automatische Handschriftenerkennung - historische und sprachwissenschaftliche Analyse

  (Third Party Funds Single)

  Project leader: Andreas Maier
  Term: October 1, 2019 - September 30, 2022
  Funding source: DFG-Einzelförderung / Sachbeihilfe (EIN-SBH)
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• Communication and Language in the Empire. The Letter Books (Briefbücher) of Nuremberg in the 15th Century: Automatic Handwriting Recognition - Historical and Linguistic Analysis

  (Third Party Funds Single)

  Project leader: Mechthild Habermann, Andreas Maier
  Term: October 1, 2019 - March 31, 2024
  Acronym: HA 1783/9
  Funding source: DFG-Einzelförderung / Sachbeihilfe (EIN-SBH)
  URL: http://lme70.informatik.uni-erlangen.de:8060/exist/apps/nuernberger-briefbuecher/projektbeschreibung.html
  Abstract

  The corporate project of historians, linguists and computer scientists aims at 1) analyzing the relevance of the imperial city of Nuremberg regarding the exchange of information in the Holy Roman Empire and 2) investigating the involvement of this urban chancellery in the development of the New High German written language. For this purpose, 3) a hybrid edition of the Nuremberg Briefbücher (letter-books) – the copied tradition of nearly all outgoing letters sent by the Small Council ruling there, ranging from 1408 to 1423 (with 844 folios altogether) – will be provided. In order to do so, 4) the existing means of automatic handwriting recognition and analysis will be further refined by new fusion methods and best practices will be developed; the results and experiences will be available for future projects and will be published as open source.With the edition of the Nuremberg Briefbücher, whose great historical and historical-linguistic value has not yet been sufficiently investigated, a unique source for the history of the city as well as of the late medieval kingdom will be made accessible. Nuremberg’s central role in the communication and in early linguistic balancing processes in the context of the formation of the New High German written language across the whole empire has repeatedly been proclaimed, however, this lacks a scientific substantiation on the basis of the existing source material. From a historical perspective, the variety of topics and the recipients of the letter books are examined as a reflection of the rich urban communication network in the early 15th century. Furthermore, the recipients of the subsequent volumes of the letterbooks will be quantified by automatic handwriting recognition. In linguistic terms, the thesis of an early supra-regionality of the Nuremberg writing language will be reviewed on the basis of a phonologically-graphematic annotation. In reciprocal cooperation with the historians, the relations to the recipients and the formulaicity of the letter books will be analyzed systematically by means of socio- and text-linguistic criteria.First experiences have already been gained in a pilot project on the oldest Nuremberg Briefbuch (1404-1408) containing about 800 letters. Concerning automatic handwriting recognition, the word error rate of the latest technology of the READ project (https://read.transkribus.eu/) will be further reduced by the new fusion procedures, which accelerates the transcription process while ensuring wider applicability.
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• Kommunikation und Sprache im Reich. Die Nürnberger Briefbücher im 15. Jahrhundert: Automatische Handschriftenerkennung - historische und sprachwissenschaftliche Analyse.

  (Third Party Funds Single)

  Project leader: Klaus Herbers, Andreas Maier, Mechthild Habermann
  Term: October 1, 2019 - September 30, 2022
  Funding source: DFG-Einzelförderung / Sachbeihilfe (EIN-SBH)
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• PPP Brasilien 2019

  (Third Party Funds Single)

  Project leader: Andreas Maier
  Term: January 1, 2019 - December 31, 2020
  Funding source: Deutscher Akademischer Austauschdienst (DAAD)
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• Deep Learning based Noise Reduction for Hearing Aids

  (Third Party Funds Single)

  Project leader: Hendrik Schröter
  Term: February 1, 2019 - January 31, 2023
  Funding source: Industrie
  Abstract

   

  Reduction of unwanted environmental noises is an important feature of today’s hearing aids, which is why noise reduction is nowadays included in almost every commercially available device. The majority of these algorithms, however, is restricted to the reduction of stationary noises. Due to the large number of different background noises in daily situations, it is hard to heuristically cover the complete solution space of noise reduction schemes. Deep learning-based algorithms pose a possible solution to this dilemma, however, they sometimes lack robustness and applicability in the strict context of hearing aids.
  In this project we investigate several deep learning.based methods for noise reduction under the constraints of modern hearing aids. This involves a low latency processing as well as the employing a hearing instrument-grade filter bank. Another important aim is the robustness of the developed methods. Therefore, the methods will be applied to real-world noise signals recorded with hearing instruments.

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• Tapping the potential of Earth Observations

  (FAU Funds)

  Project leader: Matthias Braun
  Term: April 1, 2019 - March 31, 2022
  Acronym: TAPE
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2018

• Automatic Intraoperative Tracking for Workflow and Dose Monitoring in X-Ray-based Minimally Invasive Surgeries

  (Third Party Funds Single)

  Project leader: Andreas Maier, Björn Eskofier
  Term: June 1, 2018 - May 31, 2021
  Acronym: Ait4Surgery
  Funding source: Bundesministerium für Forschung, Technologie und Raumfahrt (BMFTR)
  Abstract

  The goal of this project is the investigation of multimodal methods for the evaluation of interventional workflows in the operation room. This topic will be researched in an international project context with partners in Germany and in Brazil (UNISINOS in Porto Alegre). Methods will be developed to analyze the processes in an OR based on signals from body-worn sensors, cameras and other modalities like X-ray images recorded during the surgeries. For data analysis, techniques from the field of computer vision, machine learning and pattern recognition will be applied. The system will be integrated in a way that body-worn sensors developed by Portabiles as well as angiography systems produced by Siemens Healthcare can be included alongside.

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• Automatisiertes Intraoperatives Tracking zur Ablauf- und Dosisüberwachung in RöntgengestütztenMinimalinvasiven Eingriffen

  (Third Party Funds Group – Sub project)

  Overall project: Automatisiertes Intraoperatives Tracking zur Ablauf- und Dosisüberwachung in RöntgengestütztenMinimalinvasiven Eingriffen
  Project leader: Andreas Maier
  Term: June 1, 2018 - May 31, 2021
  Acronym: AIT4Surgery
  Funding source: Bundesministerium für Forschung, Technologie und Raumfahrt (BMFTR)
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• Deep Learning Applied to Animal Linguistics

  (FAU Funds)

  Project leader: Elmar Nöth, Christian Bergler
  Term: April 1, 2018 - April 1, 2022
  Acronym: DeepAL
  Abstract

  Deep Learning Applied to Animal Linguistics in particular the analysis of underwater audio recordings of marine animals (killer whales):

  For marine biologists, the interpretation and understanding of underwater audio recordings is essential. Based on such recordings, possible conclusions about behaviour, communication and social interactions of marine animals can be made. Despite a large number of biological studies on the subject of orca vocalizations, it is still difficult to recognize a structure or semantic/syntactic significance of orca signals in order to be able to derive any language and/or behavioral patterns. Due to a lack of techniques and computational tools, hundreds of hours of underwater recordings are still manually verified by marine biologists in order to detect potential orca vocalizations. In a post process these identified orca signals are analyzed and categorized. One of the main goals is to provide a robust and automatic method which is able to automatically detect orca calls within underwater audio recordings. A robust detection of orca signals is the baseline for any further and deeper analysis. Call type identification and classification based on pre-segmented signals can be used in order to derive semantic and syntactic patterns. In connection with the associated situational video recordings and behaviour descriptions (provided by several researchers on site) can provide potential information about communication (kind of a language model) and behaviors (e.g. hunting, socializing). Furthermore, orca signal detection can be used in conjunction with a localization software in order to provide researchers on the field with a more efficient way of searching the animals as well as individual recognition.

  For more information about the DeepAL project please contact christian.bergler@fau.de.

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• Analysis of Defects on Solar Power Cells

  (Third Party Funds Group – Sub project)

  Overall project: iPV 4.0: Intelligente vernetzte Produktion mittels Prozessrückkopplung entlang des Produktlebenszyklus von Solarmodulen
  Project leader: Andreas Maier
  Term: August 1, 2018 - July 31, 2021
  Funding source: Bundesministerium für Wirtschaft und Energie (BMWE)
  Abstract

  Over the last decade, a large number of solar power plants have been installed in Germany. To ensure a high performance, it is necessary to detect defects early. Therefore, it is required to control the quality of the solar cells during the production process, as well as to monitor the installed modules. Since manual inspections are expensive, a large degree of automation is required.
  This project aims to develop a new approach to automatically detect and classify defects on solar power cells and to estimate their impact on the performance. Further, big data methods will be applied to identify circumstances that increase the probability of a cell to become defect. As a result, it will be possible to reject cells in the production that have a high likelihood to become defect.

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• Digitalization in clinical settings using graph databases

  (Non-FAU Project)

  Project leader: Oliver Haas
  Term: since October 1, 2018
  Funding source: Bayerisches Staatsministerium für Wirtschaft, Landesentwicklung und Energie (StMWi) (seit 2018)
  Abstract

  In clinical settings, different data is stored in different systems. These data are very heterogeneous, but still highly interconnected. Graph databases are a good fit for this kind of data: they contain heterogeneous "data nodes" which can be connected to each other. The basic question is now if and how clinical data can be used in a graph database, most importantly how clinical staff can profit from this approach. Possible scenarios are a graphical user interface for clinical staff for easier access to required information or an interface for evaluation and analysis to answer more complex questions. (e.g., "Were there similar patients to this patient? How were they treated?")

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• Entwicklung eines Modellrepositoriums und einer Automatischen Schriftarterkennung für OCR-D

  (Third Party Funds Single)

  Project leader: Andreas Maier
  Term: July 1, 2018 - December 31, 2019
  Funding source: DFG-Einzelförderung / Sachbeihilfe (EIN-SBH)
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• Critical Catalogue of Luther Portraits (1519-1530)

  (Third Party Funds Group – Overall project)

  Project leader: Andreas Maier, Anselm Schubert
  Term: June 1, 2018 - May 31, 2021
  Funding source: andere Förderorganisation
  URL: https://www.gnm.de/forschung/projekte/luther-bildnisse/
  Abstract

  Quite a number of portraits of Martin Luther - known as media star of 16th century – can be found in today’s museums and libraries. However, how many portraits indeed exist and which of those are contemporary or actually date from a later period? So far unlike his works, however, the variety of contemporary portraits (painting and print) is neither completely collected nor critically analyzed. Thus, a joint project of the FAU, the Germanisches Nationalmuseum (GNM) in Nuremberg and the Technology Arts Sciences (TH Köln) was initiated. Goal of the interdisciplinary project covering art history, art technology, reformation history and computer science is the creation of a critical catalogue of Luther portraits (1519-1530). In particular, the issues of authenticity, dating of artworks and its historical usage context as well as the potential existence of serial production processes will be investigated.

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• Laboranalyse von Degradationsmechanismen unter beschleunigter Alterung und Entwicklung geeigneter feldtauglicher bildgebender Detektionsverfahren und Entwicklung und Evaluation eines Algorithmus zur Fehlerdetektion und Prognostizierung der Ausfallwahrscheinlichkeit

  (Third Party Funds Group – Overall project)

  Project leader: Andreas Maier, Christoph Brabec
  Term: August 1, 2018 - July 31, 2021
  Acronym: iPV4.0
  Funding source: Bundesministerium für Wirtschaft und Energie (BMWE)
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• Medical Image Processing for Interventional Applications

  (Third Party Funds Single)

  Project leader: Andreas Maier
  Term: January 1, 2018 - December 31, 2018
  Funding source: Virtuelle Hochschule Bayern
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• Moderner Zugang zu historischen Quellen

  (Third Party Funds Group – Sub project)

  Overall project: Moderner Zugang zu historischen Quellen
  Project leader: Andreas Maier
  Term: March 1, 2018 - February 28, 2021
  Acronym: Projekt 211
  Funding source: andere Förderorganisation
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• Radiologische und Genomische Datenanalyse zur Verbesserung der Brustkrebstherapie

  (Third Party Funds Single)

  Project leader: Andreas Maier
  Term: January 1, 2018 - December 31, 2019
  Acronym: BIG-THERA
  Funding source: Bundesministerium für Forschung, Technologie und Raumfahrt (BMFTR)
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• Similarity learning for art analysis

  (Third Party Funds Group – Sub project)

  Overall project: Critical Catalogue of Luther Portraits (1519-1530)
  Project leader: Andreas Maier
  Term: June 1, 2018 - February 28, 2021
  Funding source: andere Förderorganisation
  URL: https://www.gnm.de/forschung/forschungsprojekte/luther-bildnisse/
  Abstract

  The analysis of the similarity of portraits is an important issue for many sciences such as art history or digital humanities, as for instance it might give hints concerning serial production processes, authenticity or temporal and contextual classification of the artworks.
  In the project, first algorithms will be developed for cross-genre and multi-modal registration of portraits to overlay digitized paintings and prints as well as paintings acquired with different imaging systems such as visual light photography and infrared reflectography. Then, methods will be developed to objectively analyze the portraits according to their similarity.
  This project is part of a joint project of the FAU, the Germanisches Nationalmuseum (GNM) in Nuremberg and the Technology Arts Sciences (TH Köln) in Cologne. Goal of the interdisciplinary project covering art history, art technology, reformation history and computer science is the creation of a critical catalogue of Luther portraits (1519-1530).

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2017

• 3-D Multi-Contrast CINE Cardiac Magnetic Resonance Imaging

  (Non-FAU Project)

  Project leader: Andreas Maier
  Term: October 1, 2017 - September 30, 2020
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• Deep Learning for Multi-modal Cardiac MR Image Analysis and Quantification

  (Third Party Funds Single)

  Project leader: Sulaiman Vesal
  Term: January 1, 2017 - May 1, 2020
  Funding source: Deutscher Akademischer Austauschdienst (DAAD)
  Abstract

  Cardiovascular diseases (CVDs) and other cardiac pathologies are the leading cause of death in Europe and the USA. Timely diagnosis and post-treatment follow-ups are imperative for improving survival rates and delivering high-quality patient care. These steps rely heavily on numerous cardiac imaging modalities, which include CT (computerized tomography), coronary angiography and cardiac MRI. Cardiac MRI is a non-invasive imaging modality used to detect and monitor cardiovascular diseases. Consequently, quantitative assessment and analysis of cardiac images is vital for diagnosis and devising suitable treatments. The reliability of quantitative metrics that characterize cardiac functions such as, myocardial deformation and ventricular ejection fraction, depends heavily on the precision of the heart chamber segmentation and quantification. In this project, we aim to investigate deep learning methods to improve the diagnosis and prognosis for CVDs,

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• Development of multi-modal, multi-scale imaging framework for the early diagnosis of breast cancer

  (FAU Funds)

  Project leader: Andreas Maier, Sulaiman Vesal
  Term: March 1, 2017 - June 30, 2020
  Abstract

  Breast cancer is the leading cause of cancer related deaths in women, the second most common cancer worldwide. The development and progression of breast cancer is a dynamic biological and evolutionary process. It involves a composite organ system, with transcriptome shaped by gene aberrations, epigenetic changes, the cellular biological context, and environmental influences. Breast cancer growth and response to treatment has a number of characteristics that are specific to the individual patient, for example the response of the immune system and the interaction with the neighboring tissue. The overall complexity of breast cancer is the main cause for the current, unsatisfying understanding of its development and the patient’s therapy response. Although recent precision medicine approaches, including genomic characterization and immunotherapies, have shown clear improvements with regard to prognosis, the right treatment of this disease remains a serious challenge. The vision of the BIG-THERA team is to improve individualized breast cancer diagnostics and therapy, with the ultimate goal of extending the life expectancy of breast cancer sufferers. Our primary contribution in this regard is developing a multi-modal, multi-scale framework for the early diagnosis of the molecular sub-types of breast cancer, in a manner that supplements the clinical diagnostic workflow and enables the early identification of patients compatible with specific immunotherapeutic solutions.

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• Digital Pathology - New Approaches to the Automated Image Analysis of Histologic Slides

  (Own Funds)

  Project leader: Andreas Maier, Marc Aubreville
  Term: since January 16, 2017
  Abstract

  The pathologist is still the gold standard in the diagnosis of diseases in tissue slides. Due to its human nature, the pathologist is on one side able to flexibly adapt to the high morphological and technical variability of histologic slides but of limited objectivity due to cognitive and visual traps.

  In diverse project we are applying and validating currently available tools and solutions in digital pathology but are also developing new solution in automated image analysis to complement and improve the pathologist especially in areas of quantitative image analysis.

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• Integrative 'Big Data Modeling' for the development of novel therapeutic approaches for breast cancer

  (FAU Funds)

  Project leader: Diana Dudziak
  Term: January 1, 2017 - June 30, 2020
  Acronym: BIG-THERA
  Abstract

  Brustkrebs ist die häufigste Ursache für den Krebstod bei Frauen, die zweithäufigste Krebsart weltweit und die fünfthäufigste Ursache für krebsbedingte Todesfälle. Die Entwicklung und der Fortschritt von Brustkrebs ist ein dynamischer biologischer und evolutionärer Prozess. Es handelt sich um ein komplexes Organsystem, dessen Transkriptom durch Genaberrationen, epigenetische Veränderungen, dem zellulären biologischen Kontext und Umwelteinflüsse geprägt ist. Das Wachstum von Brustkrebs und die Reaktion auf die Behandlung hat eine Reihe von Eigenschaften, die für den einzelnen Patienten spezifisch sind, zum Beispiel die Reaktion des Immunsystems und die Interaktion mit dem benachbarten Gewebe. Die Gesamtkomplexität des Brustkrebses ist die Hauptursache für das aktuelle, unbefriedigende Verständnis seiner Entwicklung und des Therapieansprechens des Patienten. Obwohl die jüngsten präzisionsmedizinischen Ansätze, einschließlich genomischer Charakterisierung und Immuntherapien, deutliche Verbesserungen in der Prognose gezeigt haben, bleibt die richtige Behandlung dieser Krankheit eine große Herausforderung. Die Vision des BIG-THERA-Teams ist es, die individuelle Diagnose und Therapie von Brustkrebs zu verbessern, mit dem Ziel, die Lebenserwartung dieser Patienten zu verlängern.

  Folgende Ziele hat sich das BIG-THERA-Team gesetzt:

  • die Verfahren zur nicht-invasiven Früherkennung und Therapieverfolgung auf der Grundlage der Magnetresonanztomographie (MRT) zu verbessern
  • das Zusammenspiel zwischen dem Immunsystem und dem Krebswachstum zur Trennung immunologisch unterschiedlicher Brustkrebs-Subtypen für das Immuntherapie-Design aufzuklären
  • neue Strategien für die Immunphänotypisierung von Tumoren mit nanomedizinischen Techniken zu entwickeln
  • ethische Herausforderungen im Zusammenhang mit den neuen Fortschritten in der Brustkrebsforschung zu lösen
  • therapeutische Entscheidungen unter Verwendung von Big-Data Datensätzen und Informationen aus in vitro, in vivo und in silico OMICs Studien, Bildgebung und Modellierung basieren, zu optimieren.
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• Joint Iterative Reconstruction and Motion Compensation for Optical Coherence Tomography Angiography

  (Third Party Funds Single)

  Project leader: Andreas Maier, Stefan Ploner
  Term: August 1, 2017 - July 31, 2019
  Acronym: Joint Reco & MoCo for OCT(A)
  Funding source: DFG-Einzelförderung / Sachbeihilfe (EIN-SBH)
  Abstract

  Optical coherence tomography (OCT) is a non-invasive 3-D optical imagingmodality that is a standard of care in ophthalmology [1,2]. Since the introduction of Fourier-domain OCT [3], dramatic increases in imaging speedbecame possible, enabling 3-D volumetric data to be acquired. Typically, aregion of the retina is scanned line by line, where each scanned lineacquires a cross-sectional image or a B-scan. Since B-scans are acquiredin milliseconds, slices extracted along a scan line, or the fast scanaxis, are barely affected by motion. In contrast, slices extractedorthogonally to scan lines, i. e. in slow scan direction, areaffected by various types of eye motion occurring throughout the full,multi-second volume acquisition time. The most relevant types of eyemovements during acquisition are (micro-)saccades, which can introducediscontinuities or gaps between B-scans, and slow drifts, which causesmall, slowly changing distortion [4]. Additional eye motion is caused by pulsatile blood flow,respiration and head motion. Despite ongoing advances in instrumentscanning speed [5,6] typical volume acquisition times havenot decreased. Instead, the additional scanning speed is used for densevolumetric scanning or wider fields of view [7]. OCT angiography (OCTA) [8–11] multiplies therequired number of scans by at least two, and even more scans are neededto accommodate recent developments in blood flow speed estimation whichare based on multiple interscan times [12,13]. As a consequence,there is an ongoing need for improvement in motion compensation especiallyin pathology [14–16].

  We develop novel methods for retrospective motion correction of OCT volume scans of the anterior and posterior eye, and widefield imaging. Our algorithms are clinically usable due to their suitability for patients with limited fixation capabilities and increased amount of motion, due to their fast processing speed, and their high accuracy, both in terms of alignment and motion correction. By merging multiple accurately aligned scans, image quality can be increased substantially, enabling the inspection of novel features.

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• Verbesserte Charakterisierung des Versagensverhaltens von Blechwerkstoffen durch den Einsatz von Mustererkennungsmethoden

  (Third Party Funds Single)

  Project leader: Andreas Maier
  Term: April 1, 2017 - March 31, 2019
  Funding source: DFG-Einzelförderung / Sachbeihilfe (EIN-SBH)
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2016

• Intraoperative brain shift compensation and point-based vascular registration

  (Non-FAU Project)

  Project leader: Andreas Maier, Siming Bayer
  Term: May 1, 2016 - October 31, 2019
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• CODE

  (Third Party Funds Single)

  Project leader: Andreas Maier
  Term: December 1, 2016 - November 30, 2017
  Acronym: CODE
  Funding source: Industrie
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• Computer-based motive assessment

  (Own Funds)

  Project leader: Oliver Schultheiss
  Term: since January 1, 2016
  Abstract

  The standard method of measuring motives -- coding imaginative stories for motivational themes -- places a heavy burden on researchers in terms of the time and the personnel invested in this task. We collaborate with colleagues from lingusitics and computer science on the development of computer-based, automated procedures for assessing implicit motivational needs in written text. To this purpose, we use standard psycholinguistic procedures such as the Lingusitic Inquiry and Word Count software as well as sophisticated pattern recognition approaches.

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• Digital, Semantic and Physical Analysis of Media Integrity

  (Third Party Funds Single)

  Project leader: Andreas Maier
  Term: May 24, 2016 - May 23, 2017
  Acronym: DISPARITY
  Funding source: Industrie
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• Iterative Rekonstruktionsmethoden mit Fokus auf abdominelle MR-Bildgebung

  (Third Party Funds Single)

  Project leader: Andreas Maier
  Term: December 1, 2016 - April 30, 2017
  Acronym: abdominale MR-Bildgbeung
  Funding source: Siemens AG
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• Medical Image Processing for Diagnostic Applications

  (Third Party Funds Single)

  Project leader: Andreas Maier
  Term: June 1, 2016 - May 31, 2017
  Funding source: Virtuelle Hochschule Bayern
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• Modelbasierte Röntgenbildgebung

  (Third Party Funds Single)

  Project leader: Andreas Maier
  Term: February 1, 2016 - January 31, 2019
  Acronym: Patient Model
  Funding source: Siemens AG
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• Nichtrigide Registrierung von 3D DSA mit präoperativen Volumendaten, um intraoperativen Brainshift bei offender Schädel-OP zu korrigieren

  (Third Party Funds Single)

  Project leader: Andreas Maier
  Term: June 1, 2016 - May 31, 2019
  Acronym: 3D DSA
  Funding source: Siemens AG
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• Nutzung von Rohdaten-Redundanzen in der Kegelstrahl-CT

  (Third Party Funds Single)

  Project leader: Andreas Maier
  Term: May 1, 2016 - April 30, 2019
  Acronym: Rohdaten-Redundanzen
  Funding source: Siemens AG
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• Predicitve Prevention and personalized Interventional Stroke Therapy

  (Third Party Funds Group – Sub project)

  Overall project: Predicitve Prevention and personalized Interventional Stroke Therapy
  Project leader: Andreas Maier
  Term: January 1, 2016 - December 31, 2018
  Acronym: P3-Stroke
  Funding source: EU - 8. Rahmenprogramm - Horizon 2020
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• Quantifizierung der Fett-Säuren-Zusammensetzung in der Leber sowie Optimierung der zugehörigen Akquisitions- und Rekonstruktionstechniken

  (Third Party Funds Single)

  Project leader: Andreas Maier
  Term: June 15, 2016 - June 14, 2019
  Acronym: Fett-Säuren-Zusammensetzung
  Funding source: Siemens AG
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• Quantitative diagnostic dual energy CT with atlas-based prior knowledge

  (Third Party Funds Single)

  Project leader: Andreas Maier
  Term: January 1, 2016 - May 31, 2019
  Funding source: DFG-Einzelförderung / Sachbeihilfe (EIN-SBH)
  Abstract

                                    During the last decade, dual energy CT (DECT) became widely available in clinical routine. Offered by all major CT manufacturers, with differing hard- and software concepts, the DECT applications are alike: the acquired DECT data are used to conduct two- or multi material decompositions, e.g. to separate iodine and bone from soft tissue or to quantify contrast agent and fat, to classify or characterize tissue, or to increase contrasts (CNR maximization), or to suppress contrasts (artifact reduction). The applications are designed to work with certain organs and the user needs to take care to invoke the correct application and to interpret its output only in the appropriate organ or anatomical region. E.g. interpreting the output of a kidney stone applications in organs other than the kidney will yield a wrong classification. To obtain quantitative results the applications require to set patient-specific parameters. In order to calibrate those the user is asked to place ROIs in predefined anatomical regions. Since this is time-consuming users are often tempted to use the default settings instead of optimizing them. Here, we want to develop a DECT atlas to utilize its anatomical (and functional) information for con-text-sensitive DECT imaging and material decomposition, and to be able to automatically calibrate the open parameters without the need of user interaction. To improve quantification the initial images shall not be reconstructed separately but rather undergo a rawdata-based decomposition before being converted into image domain. A dedicated user interface shall be developed to provide the new context-sensitive DECT information - such as automatically decomposing each organ into different but reasonable basis materials, for example - and to display it to the reader in a convenient way. Similarly, user-placed ROIs shall trigger a context-sensitive statistical evaluation of the ROI's contents and provide it to the user. This will help to quantify the iodine uptake in a tumor or a lesion, to separate it from fat or calcium components, to estimate its blood supply etc. Since the DECT data display the contrast uptake just for a given instance in time and since this contrast depends on patient-specific factors such as the cardiac output, we are planning to normalize the contrast uptake with the help of the dual energy information contained in the atlas. This will minimize inter and intra patient effects and increase the reproducibility. In addition, organ-specific material scores shall be developed that quantify a patient's material composition on an organ by organ basis. The new methods (DECT atlas, material decomposition, ...) shall be tested and evaluated using phantom and patient studies, and shall be optimized accordingly.                             

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• Studie zum Thema "Defektspalten/Defektreihen"

  (Third Party Funds Single)

  Project leader: Andreas Maier
  Term: August 1, 2016 - January 31, 2017
  Acronym: Defektspalten
  Funding source: Industrie
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• Weiterentwicklung in der interferometrischen Röntgenbildgebung

  (Third Party Funds Single)

  Project leader: Andreas Maier
  Term: July 1, 2016 - June 30, 2019
  Acronym: Interferometrische Röntgenbildgebung
  Funding source: Siemens AG
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• Workshop "Mobile eye imaging and remote diagnosis based on the captured image"

  (Third Party Funds Single)

  Project leader: Andreas Maier
  Term: October 10, 2016 - October 14, 2016
  Acronym: Workshop
  Funding source: Industrie
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• Zusammenarbeit auf dem Gebiet der 3D-Modellierung von Koronararterien

  (Third Party Funds Single)

  Project leader: Andreas Maier
  Term: June 13, 2016 - December 31, 2017
  Acronym: Koronararterien
  Funding source: Siemens AG
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• Zusammenarbeit auf dem Gebiet der Navigationsunterstützung in röhrenförmigen Strukturen

  (Third Party Funds Single)

  Project leader: Andreas Maier
  Term: June 1, 2016 - May 31, 2019
  Acronym: Navigationsunterstützung
  Funding source: Siemens AG
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2015

• Auto ASPECTS

  (Third Party Funds Single)

  Project leader: Andreas Maier
  Term: December 1, 2015 - May 31, 2016
  Acronym: Auto ASPECTS
  Funding source: Industrie
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• Bildverbesserung der 4D DSA und Flußquantifizierung mittels 4D DSA

  (Third Party Funds Single)

  Project leader: Andreas Maier
  Term: June 15, 2015 - June 14, 2017
  Acronym: 4D DSA
  Funding source: Siemens AG
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• Helical 3-D X-ray Dark-field Imaging

  (Third Party Funds Single)

  Project leader: Andreas Maier
  Term: April 1, 2015 - March 31, 2019
  Funding source: DFG-Einzelförderung / Sachbeihilfe (EIN-SBH)
  Abstract

  The dark-field signal of an X-ray phase-contrast system captures the small-angle scattering of microscopic structures. It is acquired using Talbot-Lau interferometer, and a conventional X-ray source and a conventional X-ray detector. Interestingly, the measured intensity of the dark-field signal depends on the orientation of the microstructure. Using algorithms from tomographic image reconstruction, it is possible to recover these structure orientations. The size of the imaged structures can be considerably smaller than the resolution of the used X-ray detector. Hence, it is possible to investigate structural properties of - for example - bones or soft tissue at an unprecedented level of detail.Existing methods for 3-D dark-field reconstruction require sampling in all three spatial dimensions. For practical use, this procedure is infeasible.The goal of the proposed project is to develop a system and a method for 3-D reconstruction of structure orientations based on measurements from a practical imaging trajectory. To this end, we propose to use a helical trajectory, a concept that has been applied in conventional CT imaging with tremendous success. As a result, it will be possible for the first time to compute dark-field volumes from a practically feasible, continuous imaging trajectory. The trajectory does not require multiple rotations of the object or the patient and avoids unnecessarily long path lengths.The project will be conducted in cooperation between the experimental physics and the computer science department. The project is composed of six parts:- A: Development of a 3-D cone-beam scattering projection model- B: Development of reconstruction algorithms for a helical dark-field imaging system- C: Evaluation and optimization of the reconstruction methods towards clinical applications- D: Design of an experimental helical imaging system- E: Setup of the helical imaging system- F: Evaluation and optimization of the system performanceParts A to C will be performed by the computer science department. Parts D to E will be conducted by the experimental physics department.
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• Endovaskuläre Versorgung von Aortenaneurysmen

  (Third Party Funds Single)

  Project leader: Andreas Maier
  Term: December 1, 2015 - November 30, 2018
  Acronym: EVAR
  Funding source: Industrie
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• Feature-basierte Bildregistrierung für interventionelle Anwendungen

  (Third Party Funds Single)

  Project leader: Andreas Maier
  Term: July 1, 2015 - June 30, 2018
  Acronym: Interventionelle Anwendungen
  Funding source: Siemens AG
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• Forschungskostenzuschuss Dr. Huang, Xiaolin

  (Third Party Funds Single)

  Project leader: Andreas Maier
  Term: June 1, 2015 - May 31, 2017
  Funding source: Alexander von Humboldt-Stiftung
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• Kalibrierung von Time-of-Flight Kameras

  (Third Party Funds Single)

  Project leader: Andreas Maier
  Term: October 1, 2015 - March 31, 2017
  Acronym: Time-of-Flight Kameras 2
  Funding source: Stiftungen
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• Consistency Conditions for Artifact Reduction in Cone-beam CT

  (Third Party Funds Single)

  Project leader: Andreas Maier
  Term: since January 1, 2015
  Funding source: DFG-Einzelförderung / Sachbeihilfe (EIN-SBH)
  Abstract

  Tomographic reconstruction is the enabling technology for a wide range of transmission-based 3D imaging modalities, most notably X-ray Computed Tomography (CT). The first CT scanners built in the 70ies used parallel geometries. In order to speed up acquisition, the systems soon moved to fan-beam geometries and a much faster rotation speed. Today´s CT systems rotate four times per second and use a cone-beam geometry. This is fast enough to cover even complex organ motion such as the beating heart. However, there exists a large class of specialized CT systems that are not able to perform such fast scans. Systems using a flat-panel detector, as they are employed in C-arm angiography systems, on-board imaging systems in radiation therapy, or mobile C-arm systems, face mechanical challenges as they were mainly built to perform 2D imaging. About 15 years ago flat-detector scanners have been enabled to acquire three dimensional data. 3D imaging on these systems, however, is challenging due to their slower acquisition speed between five seconds and one minute and a small field-of-view (FOV) with a diameter of 25 to 40 cm. These drawbacks are related to the scanners´ design as highly specialized modalities. In contrast to other disadvantages of flat panel detectors like increased X-ray scattering and limited dynamic range, they will not be remedied by hardware evolution in the foreseeable future, e.g. faster motion is impossible because of the risk of collisions in the operation room. As a result, Flat-Detector Computed Tomography (FDCT) will continue to be more susceptible to artifacts in the reconstructed image due to motion and truncation. The goal of this project is to extend existing data consistency conditions, which can be practically used for FDCT to remedy intrinsic weaknesses of FDCT imaging, most importantly motion and truncation. Our goal is the practical applicability on clinical data. Thus, the new algorithms will be tested on physical phantom and patient data acquired on real FDCT scanners of our project partners. Our long-term vision behind this project is to find a concise and complete formulation for all redundancies within FDCT projection data for general trajectories and fully exploit them in the reconstruction process. Redundancies are inherent to every FDCT scan done in today´s clinical practice, but they are ignored entirely as a source of information. Data consistency conditions do not require any additional effort during the acquisitions and only little prior knowledge such as the object extent or even no assumptions about the underlying object, unlike for example total variation regularization in iterative reconstruction. Hence, they rely solely on information which is naturally present in the data.
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• Kontrast- und katheterbasierte 3D-/2D-Registrierung

  (Third Party Funds Single)

  Project leader: Andreas Maier
  Term: January 1, 2015 - September 30, 2015
  Acronym: 3D-/2D-Registrierung
  Funding source: Siemens AG
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• Segmentierung von MR-Daten in der Herzbildgebung zur Verwendung bei Interventionen an Angiographiegeräten

  (Third Party Funds Single)

  Project leader: Andreas Maier
  Term: October 1, 2015 - September 30, 2018
  Acronym: Segmentierung MR-Daten
  Funding source: Siemens AG
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• Verbesserung Freiraumerkennung/fusion im Grid: Odometrie aus Umgebungssensoren

  (Third Party Funds Single)

  Project leader: Andreas Maier
  Term: June 12, 2015 - May 31, 2016
  Acronym: Freiraumerkennung
  Funding source: Industrie
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• Weight-Bearing Image of the Knee Using A-Arm CT

  (Third Party Funds Single)

  Project leader: Andreas Maier
  Term: April 1, 2015 - February 28, 2019
  Funding source: National Institutes of Health (NIH)
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2014

• 4D Herzbildgebung

  (Third Party Funds Single)

  Project leader: Andreas Maier
  Term: February 1, 2014 - January 31, 2018
  Funding source: Siemens AG
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• Automatic classification and image analysis of confocal laser endomicroscopy images

  (Own Funds)

  Project leader: Marc Aubreville, Andreas Maier
  Term: since October 1, 2014
  Abstract

  The goal of this project is to detect cancerous tissue in confocal lasermicroendoscopy (CLE) images of the oral cavity and the vocal cord. The current treatment of these diseases is a histological analysis of specimen and a surgical resection, which has a rather high long-term survival rate, or radiation therapy with a lower survival rate. An early detection of cancerous tissue could lead to a lowered complication rate for further treatment, as well as a better overall prognosis for patients. Further, an in-vivo diagnosis during operation could narrow down the area for the necessary surgical excision, which is especially beneficial for cancer of the vocal cords.

  For this reason, we are applying methods of pattern recognition to facilitate and support diagnosis. We were able to show that these can be applied with high accuracies on CLE images.

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• Magnetresonanz am Herzen

  (Third Party Funds Single)

  Project leader: Andreas Maier, Joachim Hornegger
  Term: March 1, 2014 - June 30, 2017
  Funding source: Siemens AG
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2013

• Bewegungskompensation für Überlagerungen in der interventionellen C-Bogen Bildgebung

  (Third Party Funds Single)

  Project leader: Andreas Maier, Joachim Hornegger
  Term: June 1, 2013 - November 30, 2016
  Acronym: C-Bogen Bildgebung
  Funding source: Siemens AG
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2012

• RTG 1773: Heterogeneous Image Systems, Project C1

  (Third Party Funds Group – Sub project)

  Overall project: GRK 1773: Heterogene Bildsysteme
  Project leader: Andreas Maier
  Term: October 1, 2012 - March 31, 2017
  Funding source: DFG / Graduiertenkolleg (GRK)
  Abstract

  Especially in aging populations, Osteoarthritis (OA) is one of the leading causes for disability and functional decline of the body. Yet, the causes and progression of OA, particularly in the early stages, remain poorly understood. Current OA imaging measures require long scan times and are logistically challenging. Furthermore they are often insensitive to early changes of the tissue.

  The overarching goal of this project is the development of a novel computed tomography imaging system allowing for an analysis of the knee cartilage and menisci under weight-bearing conditions. The articular cartilage deformation under different weight-bearing conditions reveals information about abnormal motion patterns, which can be an early indicator for arthritis. This can help to detect the medical condition at an early stage.

  To allow for a scan in standing or squatting position, we opted for a C-arm CT device that can be almost arbitrarily positioned in space. The standard application area for C-arm CT is in the interventional suite, where it usually acquires images using a vertical trajectory around the patient. For the recording of the knees in this project, a horizontal trajectory has been developed.

  Scanning in standing or squatting position makes an analysis of the knee joint under weight-bearing conditions possible. However, it will also lead to involuntary motion of the knees during the scan. The motion will result in artifacts in the reconstruction that reduce the diagnostic image quality. Therefore, the goal of this project is to estimate the patient motion during the scan to reduce these artifacts. One approach is to compute the motion field of the knee using surface cameras and use the result for motion correction. Another possible approach is the design and evaluation of a biomechanical model of the knee using inertial sensors to compensate for movement.

  After the correction of the motion artifacts, the reconstructed volume is used for the segmentation and quantitative analysis of the knee joint tissue. This will give information about the risk or the progression of an arthrosis disease.

   

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2010

• Automatische Analyse von Lautbildungsstörungen bei Kindern und Jugendlichen mit Lippen-Kiefer-Gaumenspalten (LKG)

  (Third Party Funds Single)

  Project leader: Andreas Maier, Elmar Nöth
  Term: April 1, 2010 - March 31, 2013
  Funding source: DFG-Einzelförderung / Sachbeihilfe (EIN-SBH)
  Abstract

  Zur Bewertung von Sprechstörungen von Patienten mit Lippen-Kiefer-Gaumenspalten fehlen bisher objektive, validierte und einfache Verfahren. Im klinischen Alltag werden Lautbildungsstörungen bisher üblicherweise durch eine subjektive, auditive Bewertung erfasst. Diese ist für die klinische und v.a. wissenschaftliche Nutzung nur bedingt geeignet. Die automatische Sprachanalyse, wie sie für Spracherkennungssysteme genutzt wird, hat sich bereits bei Stimmstörungen als objektive Methode der globalen Bewertung erwiesen, nämlich zur Quantifizierung der Verständlichkeit. Dies ließ sich in Vorarbeiten auch auf Sprachaufnahmen von Kindern mit Lippen-Kiefer-Gaumenspalten übertragen. In dem vorliegenden Projekt wird ein Verfahren zur automatischen Unterscheidung und Quantifizierung verschiedener typischer Lautbildungsstörung wie Hypernasalität, Verlagerung der Artikulation und Veränderung der Artikulationsspannung bei Kindern und Jugendlichen mit Lippen-Kiefer-Gaumenspalten entwickelt und validiert. Dies stellt die Basis für die Ermittlung ihres Einflusses auf die Verständlichkeit sowie zur Erfassung der Ergebnisqualität verschiedener therapeutischer Konzepte dar.
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