Evidence map›Paper›PMID 42136110›Full record

ArticleBiotechnology and bioengineering2026

Machine Learning Models of Phase Contrast Images Predict Efficiency of Human Pluripotent Stem Cell Differentiation to Cardiomyocytes.

Austin K Feeney, Yaniv Ovadia, Aaron D Simmons, Christian Elabd, Claire J Peplinski, Frank Li, Sean P Palecek

Abstract read
In one paragraph

Article in Biotechnology and bioengineering, 2026. 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

7 authors.

Austin K FeeneyDepartment of Biomedical Engineering, University of Wisconsin-Madison, Madison, Wisconsin, USA.
Yaniv OvadiaStately Bio Inc., Palo Alto, California, USA.
Aaron D SimmonsDepartment of Chemical and Biological Engineering, University of Wisconsin-Madison, Madison, Wisconsin, USA.
Christian ElabdStately Bio Inc., Palo Alto, California, USA.
Claire J PeplinskiDepartment of Chemical and Biological Engineering, University of Wisconsin-Madison, Madison, Wisconsin, USA.
Frank LiStately Bio Inc., Palo Alto, California, USA.
Sean P PalecekDepartment of Chemical and Biological Engineering, University of Wisconsin-Madison, Madison, Wisconsin, USA.ORCID https://orcid.org/0000-0003-4917-5584

Funding

Biology of Aging and Age-Related Diseases Training GrantT32AG000213 · NIA · UNIVERSITY OF WISCONSIN-MADISON · PI Rozalyn M. Anderson, Sanjay Asthana · 1991 to 2026
$9.9M
Biotechnology Training ProgramT32GM135066 · NIGMS · UNIVERSITY OF WISCONSIN-MADISON · PI SCOTT M. COYLE, BRIAN G FOX · 2020 to 2026
$7.0M
Integrated Training For Physician-ScientistsT32GM140935 · NIGMS · UNIVERSITY OF WISCONSIN-MADISON · PI Anna Huttenlocher, Jeniel E Nett · 2021 to 2026
$6.5M
A Multi-Omics Approach to Discover Metabolic Critical Quality Attributes for Cardiomyocyte BiomanufacturingR01HL148059 · NHLBI · UNIVERSITY OF WISCONSIN-MADISON · PI PALECEK, SEAN P · 2019 to 2022
$1.5M
Technologies enabling robust closed-loop manufacturing of human pluripotent stem cell-derived cardiomyocytesR01HL178095 · NHLBI · UNIVERSITY OF WISCONSIN-MADISON · PI Sean P Palecek · 2025 to 2026
$1.2M
Enhancing robustness of human pluripotent stem cell differentiation to cardiomyocytes by uncovering on- and off-target differentiation trajectories via single nucleus multi-omicsF30HL173988 · NHLBI · UNIVERSITY OF WISCONSIN-MADISON · PI Austin K. Feeney · 2024 to 2026
$124k
National Science Foundation Center for Cell Manufacturing Technologies Engineering Research Center EEC-1648035NHLBI NIH HHS 1F30HL173988-01NHLBI NIH HHS 5R01HL148059NHLBI NIH HHS 5R01HL178095NHLBI NIH HHS F30 HL173988NHLBI NIH HHS R01 HL148059NHLBI NIH HHS R01 HL178095NIA NIH HHS T32 AG000213NIGMS NIH HHS T32 GM135066NIGMS NIH HHS T32 GM140935
6 · The paper itself

Abstract

Terminal cell types derived from human pluripotent stem cells (hPSCs) are at the forefront of emerging cell and gene therapy products. hPSC-derived cardiomyocytes (hPSC-CMs) are of particular interest in understanding and treating heart disease, which is highly prevalent worldwide; however, hPSC-CM manufacturing robustness is a roadblock to these applications. Non-destructive methods to monitor hPSC-CMs and predict differentiation efficiency throughout the process are needed. Here, we demonstrate a supervised machine learning approach utilizing random projection-based feature embedding and Linear Discriminant Analysis that can predict Day 12 CM purity from phase contrast images as early as 1 day after initiation of differentiation. In contrast, a heuristic based on a live-cell cTnT-GFP reporter provided limited information until Days 7-9. In summary, we provide evidence that machine learning analysis of phase contrast images is a promising approach for predicting hPSC-CM differentiation efficiency during early differentiation stages. Future efforts could use these models to inform the improvement of CM differentiation protocols and support CM biomanufacturing.

Indexed as

cardiomyocytedifferentiationhuman pluripotent stem cellmachine learningphase contrast imaging

Identifiers

PMID42136110
PMCPMC13270429

What OpenQuestion holds

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LicenceCC BY
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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.