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Content-aware Nakagami morphing for incremental brain MRI

Identifikátory výsledku

  • Kód výsledku v IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F62690094%3A18450%2F24%3A50021395" target="_blank" >RIV/62690094:18450/24:50021395 - isvavai.cz</a>

  • Výsledek na webu

    <a href="https://www.sciencedirect.com/science/article/pii/S0950705124002107?via%3Dihub" target="_blank" >https://www.sciencedirect.com/science/article/pii/S0950705124002107?via%3Dihub</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1016/j.knosys.2024.111575" target="_blank" >10.1016/j.knosys.2024.111575</a>

Alternativní jazyky

  • Jazyk výsledku

    angličtina

  • Název v původním jazyce

    Content-aware Nakagami morphing for incremental brain MRI

  • Popis výsledku v původním jazyce

    Within the carcinogenesis mechanism, from the initiation of the very first tumor cell to the preneoplastic and neoplastic cancer cell groups, cancer cells omnidirectionally and unpredictably proliferate in three-dimensional (3D) space during the promotion and progression steps. Whole tumors areas, consisting of edema, necrosis, enhancing and non-enhancing tumor subareas, could easily be identified by the typical sequences of magnetic resonance imaging (MRI), mostly by FLAIR, the fluid attenuated inversion recovery sequence. Depending on the increment value of the scanner, not every scan could be contiguous though, which might create some gaps between the slices and cause some crucial loss of information. Shape-based morphing by erosion and dilation operations might be inadequate when the source or target lesions are not found on the MRI slices, which might emerge due to unpredictable shape of tumors. Furthermore, the real trajectories and genuine shapes of the tumors in spatial view might not be seen in the planar MRI slices due to approximations during the voxel-to-pixel transformations executed in MRI devices. Therefore, we propose a novel content-aware morphing procedure to generate imaginary slices by m-parametric Nakagami imaging. The mathematical and parametric design in our framework not only leads to precise segmentation of the whole tumors according to the ground truth images; but also, to realistic morphing, based on the content of tumor footprints in MRI slices. For testing purposes, a total number of 5133 morphs are created using 1831 genuine images containing at least one lesion taken from the Brats 2012 dataset. Given the average dice score coefficients (DSC), we obtained an average of 88.44% DSC with our morphing framework outperforming the conventional dilation-based morphing result which is 83.25%. Besides being a novel morphing methodology, the outcomes of this research could also be very beneficial in smoother 3D reconstruction and more realistic volumetric calculations of lesions to help the experts working on assessment of lesions. © 2024 Elsevier B.V.

  • Název v anglickém jazyce

    Content-aware Nakagami morphing for incremental brain MRI

  • Popis výsledku anglicky

    Within the carcinogenesis mechanism, from the initiation of the very first tumor cell to the preneoplastic and neoplastic cancer cell groups, cancer cells omnidirectionally and unpredictably proliferate in three-dimensional (3D) space during the promotion and progression steps. Whole tumors areas, consisting of edema, necrosis, enhancing and non-enhancing tumor subareas, could easily be identified by the typical sequences of magnetic resonance imaging (MRI), mostly by FLAIR, the fluid attenuated inversion recovery sequence. Depending on the increment value of the scanner, not every scan could be contiguous though, which might create some gaps between the slices and cause some crucial loss of information. Shape-based morphing by erosion and dilation operations might be inadequate when the source or target lesions are not found on the MRI slices, which might emerge due to unpredictable shape of tumors. Furthermore, the real trajectories and genuine shapes of the tumors in spatial view might not be seen in the planar MRI slices due to approximations during the voxel-to-pixel transformations executed in MRI devices. Therefore, we propose a novel content-aware morphing procedure to generate imaginary slices by m-parametric Nakagami imaging. The mathematical and parametric design in our framework not only leads to precise segmentation of the whole tumors according to the ground truth images; but also, to realistic morphing, based on the content of tumor footprints in MRI slices. For testing purposes, a total number of 5133 morphs are created using 1831 genuine images containing at least one lesion taken from the Brats 2012 dataset. Given the average dice score coefficients (DSC), we obtained an average of 88.44% DSC with our morphing framework outperforming the conventional dilation-based morphing result which is 83.25%. Besides being a novel morphing methodology, the outcomes of this research could also be very beneficial in smoother 3D reconstruction and more realistic volumetric calculations of lesions to help the experts working on assessment of lesions. © 2024 Elsevier B.V.

Klasifikace

  • Druh

    J<sub>imp</sub> - Článek v periodiku v databázi Web of Science

  • CEP obor

  • OECD FORD obor

    10201 - Computer sciences, information science, bioinformathics (hardware development to be 2.2, social aspect to be 5.8)

Návaznosti výsledku

  • Projekt

  • Návaznosti

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Ostatní

  • Rok uplatnění

    2024

  • Kód důvěrnosti údajů

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Údaje specifické pro druh výsledku

  • Název periodika

    Knowledge-based systems

  • ISSN

    0950-7051

  • e-ISSN

    1872-7409

  • Svazek periodika

    291

  • Číslo periodika v rámci svazku

    May

  • Stát vydavatele periodika

    NL - Nizozemsko

  • Počet stran výsledku

    16

  • Strana od-do

    "Article number: 111575"

  • Kód UT WoS článku

    001205504400001

  • EID výsledku v databázi Scopus

    2-s2.0-85186668961