Quantifying Topology In Pancreatic Tubular Networks From Live Imaging 3D Microscopy

Research output: Contribution to journalJournal articleResearchpeer-review

Standard

Quantifying Topology In Pancreatic Tubular Networks From Live Imaging 3D Microscopy. / Arnavaz, Kasra; Krause, Oswin; Zepf, Kilian ; Bærentzen, Jakob Andreas; Miskovic Krivokapic, Jelena; Heilmann, Silja; Nyeng, Pia; Feragen, Aasa .

In: The Journal of Machine Learning for Biomedical Imaging, Vol. 2022, 015, 2022, p. 1-24.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Arnavaz, K, Krause, O, Zepf, K, Bærentzen, JA, Miskovic Krivokapic, J, Heilmann, S, Nyeng, P & Feragen, A 2022, 'Quantifying Topology In Pancreatic Tubular Networks From Live Imaging 3D Microscopy', The Journal of Machine Learning for Biomedical Imaging, vol. 2022, 015, pp. 1-24.

APA

Arnavaz, K., Krause, O., Zepf, K., Bærentzen, J. A., Miskovic Krivokapic, J., Heilmann, S., Nyeng, P., & Feragen, A. (2022). Quantifying Topology In Pancreatic Tubular Networks From Live Imaging 3D Microscopy. The Journal of Machine Learning for Biomedical Imaging, 2022, 1-24. [015].

Vancouver

Arnavaz K, Krause O, Zepf K, Bærentzen JA, Miskovic Krivokapic J, Heilmann S et al. Quantifying Topology In Pancreatic Tubular Networks From Live Imaging 3D Microscopy. The Journal of Machine Learning for Biomedical Imaging. 2022;2022:1-24. 015.

Author

Arnavaz, Kasra ; Krause, Oswin ; Zepf, Kilian ; Bærentzen, Jakob Andreas ; Miskovic Krivokapic, Jelena ; Heilmann, Silja ; Nyeng, Pia ; Feragen, Aasa . / Quantifying Topology In Pancreatic Tubular Networks From Live Imaging 3D Microscopy. In: The Journal of Machine Learning for Biomedical Imaging. 2022 ; Vol. 2022. pp. 1-24.

Bibtex

@article{02b7a79e1ba240d68179d8d51cbd0376,
title = "Quantifying Topology In Pancreatic Tubular Networks From Live Imaging 3D Microscopy",
abstract = "Motivated by the challenging segmentation task of pancreatic tubular networks, this paper tackles two commonly encountered problems in biomedical imaging: Topological consistency of the segmentation, and expensive or difficult annotation. Our contributions are the following: a) We propose a topological score which measures both topological and geometric consistency between the predicted and ground truth segmentations, applied to model selection and validation. b) We provide a full deep-learning methodology for this difficult noisy task on time-series image data. In our method, we first use a semisupervised U-net architecture, applicable to generic segmentation tasks, which jointly trains an autoencoder and a segmentation network. We then use tracking of loops over time to further improve the predicted topology. This semi-supervised approach allows us to utilize unannotated data to learn feature representations that generalize to test data with high variability, in spite of our annotated training data having very limited variation. Our contributions are validated on a challenging segmentation task, locating tubular structures in the fetal pancreas from noisy live imaging confocal microscopy. We show that our semi-supervised model outperforms not only fully supervised and pre-trained models but also an approach which takes topological consistency into account during training. Further, our approach achieves a mean loop score of 0.808 for detecting loops in the fetal pancreas, compared to a U-net trained with clDice with mean loop score 0.762.",
author = "Kasra Arnavaz and Oswin Krause and Kilian Zepf and B{\ae}rentzen, {Jakob Andreas} and {Miskovic Krivokapic}, Jelena and Silja Heilmann and Pia Nyeng and Aasa Feragen",
year = "2022",
language = "English",
volume = "2022",
pages = "1--24",
journal = "The Journal of Machine Learning for Biomedical Imaging",
issn = "2766-905X",

}

RIS

TY - JOUR

T1 - Quantifying Topology In Pancreatic Tubular Networks From Live Imaging 3D Microscopy

AU - Arnavaz, Kasra

AU - Krause, Oswin

AU - Zepf, Kilian

AU - Bærentzen, Jakob Andreas

AU - Miskovic Krivokapic, Jelena

AU - Heilmann, Silja

AU - Nyeng, Pia

AU - Feragen, Aasa

PY - 2022

Y1 - 2022

N2 - Motivated by the challenging segmentation task of pancreatic tubular networks, this paper tackles two commonly encountered problems in biomedical imaging: Topological consistency of the segmentation, and expensive or difficult annotation. Our contributions are the following: a) We propose a topological score which measures both topological and geometric consistency between the predicted and ground truth segmentations, applied to model selection and validation. b) We provide a full deep-learning methodology for this difficult noisy task on time-series image data. In our method, we first use a semisupervised U-net architecture, applicable to generic segmentation tasks, which jointly trains an autoencoder and a segmentation network. We then use tracking of loops over time to further improve the predicted topology. This semi-supervised approach allows us to utilize unannotated data to learn feature representations that generalize to test data with high variability, in spite of our annotated training data having very limited variation. Our contributions are validated on a challenging segmentation task, locating tubular structures in the fetal pancreas from noisy live imaging confocal microscopy. We show that our semi-supervised model outperforms not only fully supervised and pre-trained models but also an approach which takes topological consistency into account during training. Further, our approach achieves a mean loop score of 0.808 for detecting loops in the fetal pancreas, compared to a U-net trained with clDice with mean loop score 0.762.

AB - Motivated by the challenging segmentation task of pancreatic tubular networks, this paper tackles two commonly encountered problems in biomedical imaging: Topological consistency of the segmentation, and expensive or difficult annotation. Our contributions are the following: a) We propose a topological score which measures both topological and geometric consistency between the predicted and ground truth segmentations, applied to model selection and validation. b) We provide a full deep-learning methodology for this difficult noisy task on time-series image data. In our method, we first use a semisupervised U-net architecture, applicable to generic segmentation tasks, which jointly trains an autoencoder and a segmentation network. We then use tracking of loops over time to further improve the predicted topology. This semi-supervised approach allows us to utilize unannotated data to learn feature representations that generalize to test data with high variability, in spite of our annotated training data having very limited variation. Our contributions are validated on a challenging segmentation task, locating tubular structures in the fetal pancreas from noisy live imaging confocal microscopy. We show that our semi-supervised model outperforms not only fully supervised and pre-trained models but also an approach which takes topological consistency into account during training. Further, our approach achieves a mean loop score of 0.808 for detecting loops in the fetal pancreas, compared to a U-net trained with clDice with mean loop score 0.762.

M3 - Journal article

VL - 2022

SP - 1

EP - 24

JO - The Journal of Machine Learning for Biomedical Imaging

JF - The Journal of Machine Learning for Biomedical Imaging

SN - 2766-905X

M1 - 015

ER -

ID: 339161918