Evidence map›Paper›PMID 39215205›Full record

ArticleCommunications biology2024

UNSEG: unsupervised segmentation of cells and their nuclei in complex tissue samples.

Bogdan Kochetov, Phoenix D Bell, Paulo S Garcia, Akram S Shalaby, Rebecca Raphael, Benjamin Raymond, Brian J Leibowitz, Karen Schoedel, Rhonda M Brand, Randall E Brand and 6 more

Abstract read
In one paragraph

Article in Communications biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

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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

5 citing papers in PubMed.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

16 authors.

Bogdan KochetovDepartment of Computational and Systems Biology, University of Pittsburgh, Pittsburgh, PA, USA.ORCID 0009-0003-7463-3273
Phoenix D BellDepartment of Pathology, University of Pittsburgh, Pittsburgh, PA, USA.
Paulo S GarciaDepartment of Pathology, University of Pittsburgh, Pittsburgh, PA, USA.
Akram S ShalabyUniversity Hospitals Cleveland Medical Center, Case Western Reserve University, Cleveland, OH, USA.
Rebecca RaphaelDepartment of Computational and Systems Biology, University of Pittsburgh, Pittsburgh, PA, USA.
Benjamin RaymondDepartment of Bioengineering, University of Pittsburgh, Pittsburgh, PA, USA.
Brian J LeibowitzUPMC Hillman Cancer Center, Pittsburgh, PA, USA.
Karen SchoedelDepartment of Pathology, University of Pittsburgh, Pittsburgh, PA, USA.
Rhonda M BrandDepartment of Medicine, University of Pittsburgh, Pittsburgh, PA, USA.
Randall E BrandUPMC Hillman Cancer Center, Pittsburgh, PA, USA.
Jian YuDepartment of Medicine, University of Southern California, Los Angeles, CA, USA.ORCID 0000-0002-4021-1000
Lin ZhangDepartment of Medicine, University of Southern California, Los Angeles, CA, USA.ORCID 0000-0003-0018-3903
Brenda DiergaardeUPMC Hillman Cancer Center, Pittsburgh, PA, USA.
Robert E SchoenDepartment of Medicine, University of Pittsburgh, Pittsburgh, PA, USA.ORCID 0000-0001-7153-2766
Aatur SinghiDepartment of Pathology, University of Pittsburgh, Pittsburgh, PA, USA.
Shikhar UttamDepartment of Computational and Systems Biology, University of Pittsburgh, Pittsburgh, PA, USA. shf28@pitt.edu.ORCID 0000-0002-0897-2918

Funding

University of Pittsburgh Clinical and Translational Science InstituteUL1TR001857 · NCATS · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI REIS, STEVEN E · 2016 to 2025
$129.3M
Translation addiction and targeting in colon cancerR01CA215481 · NCI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI YU, JIAN · 2018 to 2022
$2.3M
Targeting defective necroptosis in colorectal cancerR01CA247231 · NCI · UNIVERSITY OF SOUTHERN CALIFORNIA · PI ZHANG, LIN · 2020 to 2024
$2.3M
NCATS NIH HHS UL1 TR001857U.S. Department of Health & Human Services | National Institutes of Health (NIH) UL1TR001857
6 · The paper itself

Abstract

Multiplexed imaging technologies have made it possible to interrogate complex tissue microenvironments at sub-cellular resolution within their native spatial context. However, proper quantification of this complexity requires the ability to easily and accurately segment cells into their sub-cellular compartments. Within the supervised learning paradigm, deep learning-based segmentation methods demonstrating human level performance have emerged. However, limited work has been done in developing such generalist methods within the unsupervised context. Here we present an easy-to-use unsupervised segmentation (UNSEG) method that achieves deep learning level performance without requiring any training data via leveraging a Bayesian-like framework, and nucleus and cell membrane markers. We show that UNSEG is internally consistent and better at generalizing to the complexity of tissue morphology than current deep learning methods, allowing it to unambiguously identify the cytoplasmic compartment of a cell, and localize molecules to their correct sub-cellular compartment. We also introduce a perturbed watershed algorithm for stably and automatically segmenting a cluster of cell nuclei into individual nuclei that increases the accuracy of classical watershed. Finally, we demonstrate the efficacy of UNSEG on a high-quality annotated gastrointestinal tissue dataset we have generated, on publicly available datasets, and in a range of practical scenarios.

Indexed as

Cell NucleusDeep LearningAlgorithmsBayes TheoremHumansImage Processing, Computer-AssistedUnsupervised Machine Learning

Identifiers

PMID39215205
PMCPMC11364851

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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.