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@INPROCEEDINGS{Schiffer:1043518,
author = {Schiffer, Christian and Boztoprak, Zeynep and Kropp,
Jan-Oliver and Thönnißen, Julia and Behr, Katja and
Spitzer, Hannah and Amunts, Katrin and Dickscheid, Timo},
title = {{C}yto{N}et: {A} {F}oundation {M}odel for
{C}ytoarchitecture in the {H}uman {C}erebral {C}ortex},
reportid = {FZJ-2025-02894},
year = {2025},
abstract = {Microscopic analysis of cytoarchitecture in the human
cerebral cortex plays a central role for developing
high-resolution microstructural human brain atlases.
Cytoarchitecture is defined by the spatial organization of
cells, including their shape, density, size, type, and their
columnar and laminar arrangement, which varies between brain
regions. Cytoarchitecture provides an important
microstructural reference for brain connectivity and
function and is therefore of great interest in brain
research. Microscopic scans of histological human brain
sections allow detailed analysis of cytoarchitecture.
High-throughput microscopy scanners can digitize sections of
an entire brain at 1 micrometer isotropic resolution in
about a year, resulting in petabyte-scale image datasets
that capture the brain’s complexity and variability across
multiple subjects. These large imaging datasets offer great
opportunities for brain research, but also pose novel
methodological and technical challenges that require
developing new analytical methods.Addressing these needs, we
present CytoNet, a foundation model for cytoarchitecture in
the human cerebral cortex. CytoNet is trained with a novel
self-supervised learning task that promotes the extraction
of cytoarchitectonic features from microscopic image patches
extracted along the cortical ribbon. We demonstrate that
CytoNet learns to extract powerful and anatomically
plausible representations of cytoarchitecture that capture
intra-subject variance and inter-subject variability.
CytoNet is able to compute features that are 1) completely
data-driven, 2) globally comparable across brain regions and
subjects, 3) encode a wide range of cytoarchitectonic
properties that facilitate relevant downstream analysis and
whole-brain correlative analysis, and 4) can be computed at
arbitrarily dense sampling intervals at any location within
the cerebral cortex of any subject. CytoNet achieves
state-of-the-art performance for brain area classification,
cortical layer segmentation, morphology estimation, and
data-driven discovery of cytoarchitectonic structures. Using
embedding analysis, we show that CytoNet learns to map
microscopic images into a semantically highly structured and
anatomically plausible latent space that facilitates the
aforementioned downstream tasks. Our work has broad
implications for changing the way we analyze microscopic
brain organization and will improve our ability to make
discoveries from large datasets.},
month = {Jun},
date = {2025-06-03},
organization = {Helmholtz AI Conference 2025,
Karlsruhe (Germany), 3 Jun 2025 - 5 Jun
2025},
subtyp = {After Call},
cin = {INM-1},
cid = {I:(DE-Juel1)INM-1-20090406},
pnm = {5254 - Neuroscientific Data Analytics and AI (POF4-525) /
X-BRAIN (ZT-I-PF-4-061) / Helmholtz AI - Helmholtz
Artificial Intelligence Coordination Unit – Local Unit FZJ
(E.40401.62) / JL SMHB - Joint Lab Supercomputing and
Modeling for the Human Brain (JL SMHB-2021-2027) / EBRAINS
2.0 - EBRAINS 2.0: A Research Infrastructure to Advance
Neuroscience and Brain Health (101147319) / HIBALL -
Helmholtz International BigBrain Analytics and Learning
Laboratory (HIBALL) (InterLabs-0015)},
pid = {G:(DE-HGF)POF4-5254 / G:(DE-HGF)ZT-I-PF-4-061 /
G:(DE-Juel-1)E.40401.62 / G:(DE-Juel1)JL SMHB-2021-2027 /
G:(EU-Grant)101147319 / G:(DE-HGF)InterLabs-0015},
typ = {PUB:(DE-HGF)6},
url = {https://juser.fz-juelich.de/record/1043518},
}