• Title of article

    Cell population tracking and lineage construction with spatiotemporal context

  • Author/Authors

    Kang Li، نويسنده , , Eric D. Miller، نويسنده , , Mei Chen، نويسنده , , Takeo Kanade، نويسنده , , Lee E. Weiss، نويسنده , , Phil G. Campbell، نويسنده ,

  • Issue Information
    روزنامه با شماره پیاپی سال 2008
  • Pages
    21
  • From page
    546
  • To page
    566
  • Abstract
    Automated visual-tracking of cell populations in vitro using time-lapse phase contrast microscopy enables quantitative, systematic, and high-throughput measurements of cell behaviors. These measurements include the spatiotemporal quantification of cell migration, mitosis, apoptosis, and the reconstruction of cell lineages. The combination of low signal-to-noise ratio of phase contrast microscopy images, high and varying densities of the cell cultures, topological complexities of cell shapes, and wide range of cell behaviors poses many challenges to existing tracking techniques. This paper presents a fully automated multi-target tracking system that can efficiently cope with these challenges while simultaneously tracking and analyzing thousands of cells observed using time-lapse phase contrast microscopy. The system combines bottom-up and top-down image analysis by integrating multiple collaborative modules, which exploit a fast geometric active contour tracker in conjunction with adaptive interacting multiple models (IMM) motion filtering and spatiotemporal trajectory optimization. The system, which was tested using a variety of cell populations, achieved tracking accuracy in the range of 86.9–92.5%.
  • Keywords
    Cell trackingLevel setJump Markov systemsIMM filterQuasi-Bayes estimationLinear programmingPhase contrastTime-lapse microscopyStem ce
  • Journal title
    Medical Image Analysis
  • Serial Year
    2008
  • Journal title
    Medical Image Analysis
  • Record number

    450049