TY - GEN
T1 - A unified graphical models framework for automated human embryo tracking in time lapse microscopy
AU - Moussavi, F.
AU - Wang, Y.
AU - Lorenzen, P.
AU - Oakley, J.
AU - Russakoff, D.
AU - Gould, S.
N1 - Publisher Copyright:
© 2014 IEEE.
PY - 2014/7/29
Y1 - 2014/7/29
N2 - Time lapse microscopy has emerged as an important modality for studying early human embryo development. Detection of certain events can provide insight into embryo health and fate. Embryo tracking is challenged by a high dimensional search space, weak features, outliers, occlusions, missing data, multiple interacting deformable targets, changing topology, and a weak motion model. We address these with a data driven approach that uses a rich set of discriminative image and geometric features and their spatiotemporal context. We pose the mitosis detection problem as augmented simultaneous segmentation and classification in a conditional random field framework that combines tracking based and tracking free elements. For 275 clinical image sequences we measured division events during the first 48 hours of embryo development to within 30 minutes resulting in an improvement of 24.2% over a tracking-based approach and a 35.7% improvement over a tracking-free approach, and more than an order of magnitude improvement over a traditional particle filter, demonstrating the success of our framework.
AB - Time lapse microscopy has emerged as an important modality for studying early human embryo development. Detection of certain events can provide insight into embryo health and fate. Embryo tracking is challenged by a high dimensional search space, weak features, outliers, occlusions, missing data, multiple interacting deformable targets, changing topology, and a weak motion model. We address these with a data driven approach that uses a rich set of discriminative image and geometric features and their spatiotemporal context. We pose the mitosis detection problem as augmented simultaneous segmentation and classification in a conditional random field framework that combines tracking based and tracking free elements. For 275 clinical image sequences we measured division events during the first 48 hours of embryo development to within 30 minutes resulting in an improvement of 24.2% over a tracking-based approach and a 35.7% improvement over a tracking-free approach, and more than an order of magnitude improvement over a traditional particle filter, demonstrating the success of our framework.
UR - http://www.scopus.com/inward/record.url?scp=84927915237&partnerID=8YFLogxK
U2 - 10.1109/isbi.2014.6867872
DO - 10.1109/isbi.2014.6867872
M3 - Conference contribution
T3 - 2014 IEEE 11th International Symposium on Biomedical Imaging, ISBI 2014
SP - 314
EP - 320
BT - 2014 IEEE 11th International Symposium on Biomedical Imaging, ISBI 2014
PB - Institute of Electrical and Electronics Engineers Inc.
T2 - 2014 IEEE 11th International Symposium on Biomedical Imaging, ISBI 2014
Y2 - 29 April 2014 through 2 May 2014
ER -