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dc.contributor.authorKnötel, Daviden_US
dc.contributor.authorBecker, Carolaen_US
dc.contributor.authorScholtz, Gerharden_US
dc.contributor.authorBaum, Danielen_US
dc.contributor.editorPuig Puig, Anna and Schultz, Thomas and Vilanova, Anna and Hotz, Ingrid and Kozlikova, Barbora and Vázquez, Pere-Pauen_US
dc.date.accessioned2018-09-19T15:19:57Z
dc.date.available2018-09-19T15:19:57Z
dc.date.issued2018
dc.identifier.isbn978-3-03868-056-7
dc.identifier.issn2070-5786
dc.identifier.urihttps://diglib.eg.org:443/handle/10.2312/vcbm20181243
dc.identifier.urihttps://doi.org/10.2312/vcbm.20181243
dc.description.abstractWe show how biologically coherent mesh models of animals can be created from µCT data to generate artificial yet naturally looking intermediate objects. The whole pipeline of processing algorithms is presented, starting from generating topologically equivalent surface meshes, followed by solving the correspondence problem, and, finally, creating a surface morphing. In this pipeline, we address all the challenges that are due to dealing with complex biological, non-isometric objects. For biological objects it is often particularly important to obtain deformations that look as realistic as possible. In addition, spatially non-uniform shape morphings that only change one part of the surface and keep the rest as stable as possible are of interest for evolutionary studies, since functional modules often change independently from one another. We use Poisson interpolation for this purpose and show that it is well suited to generate both global and local shape deformations.en_US
dc.publisherThe Eurographics Associationen_US
dc.subjectCCS Concepts Computing methodologies
dc.subjectImage processing
dc.subjectMesh models
dc.subjectShape analysis
dc.subjectApplied computing
dc.subjectImaging
dc.titleGlobal and Local Mesh Morphing for Complex Biological Objects from µCT Dataen_US
dc.description.seriesinformationEurographics Workshop on Visual Computing for Biology and Medicine
dc.description.sectionheadersSurfaces
dc.identifier.doi10.2312/vcbm.20181243
dc.identifier.pages179-183


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