TY - GEN
T1 - Automatic Mouse Embryo Brain Ventricle & Body Segmentation and Mutant Classification from Ultrasound Data Using Deep Learning
AU - Qiu, Ziming
AU - Nair, Nitin
AU - Langerman, Jack
AU - Aristizabal, Orlando
AU - Mamou, Jonathan
AU - Turnbull, Daniel H.
AU - Ketterling, Jeffrey A.
AU - Wang, Yao
N1 - Funding Information:
The research described in this paper was supported in part by NIH grant EB022950.
Publisher Copyright:
© 2019 IEEE.
PY - 2019/10
Y1 - 2019/10
N2 - High-frequency ultrasound (HFU) is well suited for imaging embryonic mice in vivo because it is non-invasive and real-time. Manual segmentation of the brain ventricles (BVs) and whole body from 3D HFU images is time-consuming and requires specialized training. This paper presents a deep-learning-based segmentation pipeline which automates several time-consuming, repetitive tasks currently performed to study genetic mutations in developing mouse embryos. Namely, the pipeline accurately segments the BV and body regions in 3D HFU images of mouse embryos, despite significant challenges due to position and shape variation of the embryos, as well as imaging artifacts. Based on the BV segmentation, a 3D convolutional neural network (CNN) is further trained to detect embryos with the Engrailed-1 (En1) mutation. The algorithms achieve 0.896 and 0.925 Dice Similarity Coefficient (DSC) for BV and body segmentation, respectively, and 95.8% accuracy on mutant classification. Through gradient based interrogation and visualization of the trained classifier, it is demonstrated that the model focuses on the morphological structures known to be affected by the En1 mutation.
AB - High-frequency ultrasound (HFU) is well suited for imaging embryonic mice in vivo because it is non-invasive and real-time. Manual segmentation of the brain ventricles (BVs) and whole body from 3D HFU images is time-consuming and requires specialized training. This paper presents a deep-learning-based segmentation pipeline which automates several time-consuming, repetitive tasks currently performed to study genetic mutations in developing mouse embryos. Namely, the pipeline accurately segments the BV and body regions in 3D HFU images of mouse embryos, despite significant challenges due to position and shape variation of the embryos, as well as imaging artifacts. Based on the BV segmentation, a 3D convolutional neural network (CNN) is further trained to detect embryos with the Engrailed-1 (En1) mutation. The algorithms achieve 0.896 and 0.925 Dice Similarity Coefficient (DSC) for BV and body segmentation, respectively, and 95.8% accuracy on mutant classification. Through gradient based interrogation and visualization of the trained classifier, it is demonstrated that the model focuses on the morphological structures known to be affected by the En1 mutation.
KW - deep learning
KW - explainable ai
KW - mutant classification
KW - segmentation
KW - ultrasound
KW - visualization
UR - http://www.scopus.com/inward/record.url?scp=85077536757&partnerID=8YFLogxK
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U2 - 10.1109/ULTSYM.2019.8925720
DO - 10.1109/ULTSYM.2019.8925720
M3 - Conference contribution
AN - SCOPUS:85077536757
T3 - IEEE International Ultrasonics Symposium, IUS
SP - 12
EP - 15
BT - 2019 IEEE International Ultrasonics Symposium, IUS 2019
PB - IEEE Computer Society
T2 - 2019 IEEE International Ultrasonics Symposium, IUS 2019
Y2 - 6 October 2019 through 9 October 2019
ER -