TY - GEN
T1 - Automated monitoring of human embryonic cells up to the 5-cell stage in time-lapse microscopy images
AU - Khan, Aisha
AU - Gould, Stephen
AU - Salzmann, Mathieu
N1 - Publisher Copyright:
© 2015 IEEE.
PY - 2015/7/21
Y1 - 2015/7/21
N2 - Measurement of the proliferative behavior of human embryonic cells in vitro is important to many biomedical applications ranging from basic biology research to advanced applications, such as determining embryo viability during in vitro fertilization (IVF) treatments. Automated prediction of the embryo viability, by tracking cell divisions up to the 4-cell stage, improves embryo selection and may lead to increased success rates in IVF pregnancies. Recent research in cell biology has suggested that tracking cell divisions beyond the 4-cell stage further improves embryo selection. In the current state-of-the-art, later events (e.g., time to reach the 5-cell stage) can only be assessed manually. In this work we automatically predict the number of cells at every time point, and predict when the embryo divides beyond four cells in a time-lapse microscopy sequence. Our approach employs a conditional random field (CRF) that compactly encodes various aspects of the evolving embryo and estimates the number of cells at each time step via exact inference. We demonstrate the effectiveness of our method on a data set of 33 developing human embryos.
AB - Measurement of the proliferative behavior of human embryonic cells in vitro is important to many biomedical applications ranging from basic biology research to advanced applications, such as determining embryo viability during in vitro fertilization (IVF) treatments. Automated prediction of the embryo viability, by tracking cell divisions up to the 4-cell stage, improves embryo selection and may lead to increased success rates in IVF pregnancies. Recent research in cell biology has suggested that tracking cell divisions beyond the 4-cell stage further improves embryo selection. In the current state-of-the-art, later events (e.g., time to reach the 5-cell stage) can only be assessed manually. In this work we automatically predict the number of cells at every time point, and predict when the embryo divides beyond four cells in a time-lapse microscopy sequence. Our approach employs a conditional random field (CRF) that compactly encodes various aspects of the evolving embryo and estimates the number of cells at each time step via exact inference. We demonstrate the effectiveness of our method on a data set of 33 developing human embryos.
UR - http://www.scopus.com/inward/record.url?scp=84944327821&partnerID=8YFLogxK
U2 - 10.1109/ISBI.2015.7163894
DO - 10.1109/ISBI.2015.7163894
M3 - Conference contribution
T3 - Proceedings - International Symposium on Biomedical Imaging
SP - 389
EP - 393
BT - 2015 IEEE 12th International Symposium on Biomedical Imaging, ISBI 2015
PB - IEEE Computer Society
T2 - 12th IEEE International Symposium on Biomedical Imaging, ISBI 2015
Y2 - 16 April 2015 through 19 April 2015
ER -