Generative modeling of living cells with SO(3)-equivariant implicit neural representations

Varování

Publikace nespadá pod Ekonomicko-správní fakultu, ale pod Fakultu informatiky. Oficiální stránka publikace je na webu muni.cz.
Autoři

WIESNER David SUK Julian DUMMER Sven NEČASOVÁ Tereza VLADIMÍR Ulman SVOBODA David WOLTERINK Jelmer

Rok publikování 2024
Druh Článek v odborném periodiku
Časopis / Zdroj Medical Image Analysis
Fakulta / Pracoviště MU

Fakulta informatiky

Citace
www https://doi.org/10.1016/j.media.2023.102991
Doi http://dx.doi.org/10.1016/j.media.2023.102991
Klíčová slova cell shape modeling; neural networks; implicit neural representations; signed distance function; generative model; interpolation
Popis Data-driven cell tracking and segmentation methods in biomedical imaging require diverse and information-rich training data. In cases where the number of training samples is limited, synthetic computer-generated data sets can be used to improve these methods. This requires the synthesis of cell shapes as well as corresponding microscopy images using generative models. To synthesize realistic living cell shapes, the shape representation used by the generative model should be able to accurately represent fine details and changes in topology, which are common in cells. These requirements are not met by 3D voxel masks, which are restricted in resolution, and polygon meshes, which do not easily model processes like cell growth and mitosis. In this work, we propose to represent living cell shapes as level sets of signed distance functions (SDFs) which are estimated by neural networks. We optimize a fully-connected neural network to provide an implicit representation of the SDF value at any point in a 3D+time domain, conditioned on a learned latent code that is disentangled from the rotation of the cell shape. We demonstrate the effectiveness of this approach on cells that exhibit rapid deformations (Platynereis dumerilii), cells that grow and divide (C. elegans), and cells that have growing and branching filopodial protrusions (A549 human lung carcinoma cells). A quantitative evaluation using shape features and Dice similarity coefficients of real and synthetic cell shapes shows that our model can generate topologically plausible complex cell shapes in 3D+time with high similarity to real living cell shapes. Finally, we show how microscopy images of living cells that correspond to our generated cell shapes can be synthesized using an image-to-image model.
Související projekty:

Používáte starou verzi internetového prohlížeče. Doporučujeme aktualizovat Váš prohlížeč na nejnovější verzi.