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Träfflista för sökning "WFRF:(Ryner Martin) srt2:(2006-2009)"

Sökning: WFRF:(Ryner Martin) > (2006-2009)

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1.
  • Kylberg, Gustaf, et al. (författare)
  • Local Intensity and PCA Based Detection of Virus Particle Candidates in Transmission Electron Microscopy Images
  • 2009
  • Ingår i: Proc. 6th International Symposium on Image and Signal Processing and Analysis. - Piscataway, NJ : IEEE. - 9789531841351 ; , s. 426-431
  • Konferensbidrag (refereegranskat)abstract
    • We present a general method using local intensity informationand PCA to detect objects characterized onlyby that they differ from their surroundings. We apply ourmethod to the problem of automatically detecting virus particlecandidates in transmission electron microscopy images.Viruses have very different shapes and sizes, manyspecies are spherical whereas others are highly pleomorphic.To detect any kind of virus particles in electron microscopyimages it is therefore necessary to use a methodnot restricted to detection of a specific shape. The methodproposed here uses only one input parameter, the approximatevirus thickness, which is a conserved feature withina virus species. It is capable to detect virus particles ofvery varying shapes. Results on images with highly texturedbackground of several different virus species are presented.
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2.
  • Ryner, Martin, et al. (författare)
  • Identification and classification of human cytomegalovirus capsids in textured electron micrographs using deformed template matching
  • 2006
  • Ingår i: Virology Journal. - : Springer Science and Business Media LLC. - 1743-422X. ; 3
  • Tidskriftsartikel (refereegranskat)abstract
    • Background: Characterization of the structural morphology of virus particles in electron micrographs is a complex task, but desirable in connection with investigation of the maturation process and detection of changes in viral particle morphology in response to the effect of a mutation or antiviral drugs being applied. Therefore, we have here developed a procedure for describing and classifying virus particle forms in electron micrographs, based on determination of the invariant characteristics of the projection of a given virus structure. The template for the virus particle is created on the basis of information obtained from a small training set of electron micrographs and is then employed to classify and quantify similar structures of interest in an unlimited number of electron micrographs by a process of correlation. Results: Practical application of the method is demonstrated by the ability to locate three diverse classes of virus particles in transmission electron micrographs of fibroblasts infected with human cytomegalovirus. These results show that fast screening of the total number of viral structures at different stages of maturation in a large set of electron micrographs, a task that is otherwise both time-consuming and tedious for the expert, can be accomplished rapidly and reliably with our automated procedure. Using linear deformation analysis, this novel algorithm described here can handle capsid variations such as ellipticity and furthermore allows evaluation of properties such as the size and orientation of a virus particle. Conclusion: Our methodological procedure represents a promising objective tool for comparative studies of the intracellular assembly processes of virus particles using electron microscopy in combination with our digitized image analysis tool. An automated method for sorting and classifying virus particles at different stages of maturation will enable us to quantify virus production in all stages of the virus maturation process, not only count the number of infectious particles released from un infected cell.
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