Evidence map›Paper›PMID 40505016›Full record

ArticlePLoS computational biology2025

Uncertainty-aware traction force microscopy.

Adithan Kandasamy, Yi-Ting Yeh, Ricardo Serrano, Mark Mercola, Juan C Del Alamo

Abstract read
In one paragraph

Article in PLoS computational biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors.

Adithan KandasamyDepartment of Mechanical Engineering, University of Washington, Seattle, Washington, United States of America.ORCID 0000-0002-6713-245X
Yi-Ting YehDepartment of Mechanical Engineering, University of Washington, Seattle, Washington, United States of America.
Ricardo SerranoCardiovascular Institute and Department of Medicine, Stanford University, Stanford, California, United States of America.
Mark MercolaCardiovascular Institute and Department of Medicine, Stanford University, Stanford, California, United States of America.
Juan C Del AlamoDepartment of Mechanical Engineering, University of Washington, Seattle, Washington, United States of America.ORCID 0000-0001-5683-0239

Funding

Project 3 (Mercola)P01HL141084 · NHLBI · STANFORD UNIVERSITY · PI Joseph C. Wu · 2019 to 2026
$21.1M
Training in Myocardial Biology at Stanford (TIMBS)T32HL094274 · NHLBI · STANFORD UNIVERSITY · PI Euan A Ashley, Daniel Bernstein · 2010 to 2026
$5.0M
MicroRNA Control of Dilated CardiomyopathyR01HL130840 · NHLBI · STANFORD UNIVERSITY · PI MARK MERCOLA, Shankar Subramaniam · 2016 to 2026
$4.6M
Mechanisms by which red blood cells contribute cardiopulmonary bypass associated inflammationR01HL170607 · NHLBI · SEATTLE CHILDREN'S HOSPITAL · PI VISHAL NIGAM, Juan Carlos del Alamo · 2024 to 2026
$2.6M
Mechanisms of regulation of lymphocyte migration by actin cytoskeletal effectorsR01AI167943 · NIAID · UNIVERSITY OF COLORADO DENVER · PI Jordan Jacobelli · 2022 to 2026
$2.4M
Targeting the genotype to phenotype link in HCM as a therapeutic strategyR01HL152055 · NHLBI · STANFORD UNIVERSITY · PI MERCOLA, MARK · 2021 to 2024
$2.3M
hiPSC Modeling of Restrictive Cardiomyopathy for Drug TestingR01HL169340 · NHLBI · STANFORD UNIVERSITY · PI MARK MERCOLA · 2023 to 2026
$2.3M
Evaluation of the AMPK-BACH1-NRF2 Axis as a Therapeutic Target for Inherited DCMR01HL170080 · NHLBI · STANFORD UNIVERSITY · PI MARK MERCOLA · 2024 to 2026
$1.8M
High throughput platform for simultaneous multiparametric assessment of cardiac physiology for heart failure drug developmentR33HL167258 · NHLBI · STANFORD UNIVERSITY · PI MERCOLA, MARK · 2023 to 2024
$908k
Kinetic Imaging Cytometer (KIC) for High Throughput Studies of Cellular PhysiologyS10OD030264 · OD · STANFORD UNIVERSITY · PI MERCOLA, MARK · 2021 to 2021
$528k
NHLBI NIH HHS P01 HL141084NHLBI NIH HHS R01 HL130840NHLBI NIH HHS R01 HL152055NHLBI NIH HHS R01 HL169340NHLBI NIH HHS R01 HL170080NHLBI NIH HHS R01 HL170607NHLBI NIH HHS R33 HL167258NHLBI NIH HHS T32 HL094274NIAID NIH HHS R01 AI167943NIH HHS S10 OD030264
6 · The paper itself

Abstract

Traction Force Microscopy (TFM) is a versatile tool to quantify cell-exerted forces by imaging and tracking fiduciary markers embedded in elastic substrates. The computations involved in TFM are often ill-conditioned, and data smoothing or regularization is required to avoid overfitting the noise in the tracked displacements. Most TFM calculations depend critically on the heuristic selection of regularization (hyper-) parameters affecting the balance between overfitting and smoothing. However, TFM methods rarely estimate or account for measurement errors in substrate deformation to adjust the regularization level accordingly. Moreover, there is a lack of tools for uncertainty quantification (UQ) to understand how these errors propagate to the recovered traction stresses. These limitations make it difficult to interpret the TFM readouts and hinder comparing different experiments. This manuscript presents an uncertainty-aware TFM technique that estimates the variability in the magnitude and direction of the traction stress vector recovered at each point in space and time of each experiment. In this technique, a non-parametric bootstrap method perturbs the cross-correlation functional of Particle Image Velocimetry (PIV) to assess the uncertainty of the measured deformation. This information is passed on to a hierarchical Bayesian TFM framework with spatially adaptive regularization that propagates the uncertainty to the traction stress readouts (TFM-UQ). We evaluate TFM-UQ using synthetic datasets with prescribed image quality variations and demonstrate its application to experimental datasets. These studies show that TFM-UQ bypasses the need for subjective regularization parameter selection and locally adapts smoothing, outperforming traditional regularization methods. They also illustrate how uncertainty-aware TFM tools can be used to objectively choose key image analysis parameters like PIV window size. We anticipate that these tools will allow for decoupling biological heterogeneity from measurement variability and facilitate automating the analysis of large datasets by parameter-free, input data-based regularization.

Indexed as

Microscopy, Atomic ForceAlgorithmsComputational BiologyHumansImage Processing, Computer-AssistedUncertainty

Identifiers

PMID40505016
PMCPMC12251289

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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.