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Data fusion and smoothing for probabilistic tracking of viral structures in fluorescence microscopy images.
Ritter, C; Wollmann, T; Lee, J-Y; Imle, A; Müller, B; Fackler, O T; Bartenschlager, R; Rohr, K.
Afiliación
  • Ritter C; Biomedical Computer Vision Group, BioQuant, IPMB, Heidelberg University, Im Neuenheimer Feld 267, Heidelberg, Germany. Electronic address: christian.ritter@bioquant.uni-heidelberg.de.
  • Wollmann T; Biomedical Computer Vision Group, BioQuant, IPMB, Heidelberg University, Im Neuenheimer Feld 267, Heidelberg, Germany.
  • Lee JY; Dept. of Infectious Diseases, Molecular Virology, Heidelberg University, Im Neuenheimer Feld 344, Heidelberg, Germany; German Center for Infection Research (DZIF), Heidelberg Partner Site, Germany.
  • Imle A; Dept. of Infectious Diseases, Integrative Virology, University Hospital Heidelberg, Im Neuenheimer Feld 344, Heidelberg, Germany; Cell Biology and Biophysics Unit, European Molecular Biology Laboratory, Meyerhofstrasse 1, Heidelberg, Germany.
  • Müller B; Dept. of Infectious Diseases, Virology, University Hospital Heidelberg, Im Neuenheimer Feld 344, Heidelberg, Germany.
  • Fackler OT; Dept. of Infectious Diseases, Integrative Virology, University Hospital Heidelberg, Im Neuenheimer Feld 344, Heidelberg, Germany; German Center for Infection Research (DZIF), Heidelberg Partner Site, Germany.
  • Bartenschlager R; Dept. of Infectious Diseases, Molecular Virology, Heidelberg University, Im Neuenheimer Feld 344, Heidelberg, Germany; German Center for Infection Research (DZIF), Heidelberg Partner Site, Germany.
  • Rohr K; Biomedical Computer Vision Group, BioQuant, IPMB, Heidelberg University, Im Neuenheimer Feld 267, Heidelberg, Germany. Electronic address: k.rohr@uni-heidelberg.de.
Med Image Anal ; 73: 102168, 2021 10.
Article en En | MEDLINE | ID: mdl-34340105
ABSTRACT
Automatic tracking of viral structures displayed as small spots in fluorescence microscopy images is an important task to determine quantitative information about cellular processes. We introduce a novel probabilistic approach for tracking multiple particles based on multi-sensor data fusion and Bayesian smoothing methods. The approach exploits multiple measurements as in a particle filter, both detection-based measurements and prediction-based measurements from a Kalman filter using probabilistic data association with elliptical sampling. Compared to previous probabilistic tracking methods, our approach exploits separate uncertainties for the detection-based and prediction-based measurements, and integrates them by a sequential multi-sensor data fusion method. In addition, information from both past and future time points is taken into account by a Bayesian smoothing method in conjunction with the covariance intersection algorithm for data fusion. Also, motion information based on displacements is used to improve correspondence finding. Our approach has been evaluated on data of the Particle Tracking Challenge and yielded state-of-the-art results or outperformed previous approaches. We also applied our approach to challenging time-lapse fluorescence microscopy data of human immunodeficiency virus type 1 and hepatitis C virus proteins acquired with different types of microscopes and spatial-temporal resolutions. It turned out, that our approach outperforms existing methods.
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Algoritmos / Estructuras Virales Tipo de estudio: Prognostic_studies Límite: Humans Idioma: En Revista: Med Image Anal Asunto de la revista: DIAGNOSTICO POR IMAGEM Año: 2021 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Algoritmos / Estructuras Virales Tipo de estudio: Prognostic_studies Límite: Humans Idioma: En Revista: Med Image Anal Asunto de la revista: DIAGNOSTICO POR IMAGEM Año: 2021 Tipo del documento: Article