Evidence map›Paper›PMID 40667089›Full record

ArticlebioRxiv : the preprint server for biology2025

Morphology-Aware Profiling of Highly Multiplexed Tissue Images using Variational Autoencoders.

Gregory J Baker, Edward Novikov, Shannon Coy, Yu-An Chen, Clemens B Hug, Zergham Ahmed, Sebastián A Cajas Ordóñez, Siyu Huang, Clarence Yapp, Artem Sokolov and 3 more

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors.

Gregory J BakerLaboratory of Systems Pharmacology, Harvard Medical School, Boston, MA.ORCID 0000-0002-5196-3961
Edward NovikovLaboratory of Systems Pharmacology, Harvard Medical School, Boston, MA.ORCID 0000-0003-1476-5111
Shannon CoyLaboratory of Systems Pharmacology, Harvard Medical School, Boston, MA.ORCID 0000-0003-0033-9031
Yu-An ChenLaboratory of Systems Pharmacology, Harvard Medical School, Boston, MA.ORCID 0000-0001-7228-4696
Clemens B HugLaboratory of Systems Pharmacology, Harvard Medical School, Boston, MA.ORCID 0000-0002-8299-3274
Zergham AhmedLaboratory of Systems Pharmacology, Harvard Medical School, Boston, MA.ORCID 0000-0001-8368-0408
Sebastián A Cajas OrdóñezHarvard John A. Paulson School of Engineering and Applied Sciences, Harvard University, Cambridge, MA.ORCID 0000-0003-0579-6178
Siyu HuangHarvard John A. Paulson School of Engineering and Applied Sciences, Harvard University, Cambridge, MA.ORCID 0000-0002-2929-0115
Clarence YappLaboratory of Systems Pharmacology, Harvard Medical School, Boston, MA.ORCID 0000-0003-1144-5710
Artem SokolovLaboratory of Systems Pharmacology, Harvard Medical School, Boston, MA.ORCID 0000-0002-8056-0504
Hanspeter PfisterHarvard John A. Paulson School of Engineering and Applied Sciences, Harvard University, Cambridge, MA.ORCID 0000-0002-3620-2582
Sandro SantagataLaboratory of Systems Pharmacology, Harvard Medical School, Boston, MA.ORCID 0000-0002-7528-9668
Peter K SorgerLaboratory of Systems Pharmacology, Harvard Medical School, Boston, MA.ORCID 0000-0002-3364-1838

Funding

Pre-cancer atlases of cutaneous and hematologic origin (PATCH Center)U2CCA233262 · NCI · HARVARD MEDICAL SCHOOL · PI SANTAGATA, SANDRO · 2018 to 2023
$8.7M
Visual Analytics for Exploration and Hypothesis Generation Using Highly MultiplexedSpatial Data of Tissues and TumorsU01CA284207 · NCI · HARVARD MEDICAL SCHOOL · PI PFISTER, HANSPETER, SANTAGATA, SANDRO · 2023 to 2025
$1.4M
NCI NIH HHS U01 CA284207NCI NIH HHS U2C CA233262
6 · The paper itself

Abstract

Spatial proteomics (highly multiplexed tissue imaging) provides unprecedented insight into the types, states, and spatial organization of cells within preserved tissue environments. To enable single-cell analysis, high-plex images are typically segmented using algorithms that assign marker signals to individual cells. However, conventional segmentation is often imprecise and susceptible to signal spillover between adjacent cells, interfering with accurate cell type identification. Segmentation-based methods also fail to capture the morphological detail that histopathologists rely on for disease diagnosis and staging. Here, we present a method that combines unsupervised, pixel-level machine learning using autoencoders with traditional segmentation to generate single-cell data that captures information on protein abundance, morphology, and local neighborhood in a manner analogous to human experts while overcoming the problem of signal spillover. The result is a more accurate and nuanced characterization of cell types and states than segmentation-based analysis alone.

Indexed as

artificial intelligence (AI)cancerCyCIFMxIFspatial proteomicsvariational autoencoder (VAE)

Identifiers

PMID40667089
PMCPMC12262432

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.