Evidence map›Paper›PMID 27910869›Full record

ArticleScientific reports2016

Multiparameter mechanical and morphometric screening of cells.

Mahdokht Masaeli, Dewal Gupta, Sean O'Byrne, Henry T K Tse, Daniel R Gossett, Peter Tseng, Andrew S Utada, Hea-Jin Jung, Stephen Young, Amander T Clark and 1 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
2.8field-weighted citation impact, top 10% of its field
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

25 citing papers in PubMed, 58 citations in OpenAlex.

  1. Review
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  6. Opportunities and Challenges in Applying AI to Evolutionary Morphology.Integrative organismal biology (Oxford, England) · 2024
    Review
  7. Article
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  20. Developments in label-free microfluidic methods for single-cell analysis and sorting.Wiley interdisciplinary reviews. Nanomedicine and nanobiotechnology · 2019
    Review
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

11 authors at 3 institutions in 1 country.

Mahdokht MasaeliDepartment of Bioengineering, University of California, Los Angeles, CA, USA.
Dewal GuptaDepartment of Bioengineering, University of California, Los Angeles, CA, USA.
Sean O'ByrneDepartment of Bioengineering, University of California, Los Angeles, CA, USA.
Henry T K TseDepartment of Bioengineering, University of California, Los Angeles, CA, USA.
Daniel R GossettDepartment of Bioengineering, University of California, Los Angeles, CA, USA.
Peter TsengDepartment of Bioengineering, University of California, Los Angeles, CA, USA.
Andrew S UtadaDepartment of Bioengineering, University of California, Los Angeles, CA, USA.
Hea-Jin JungMolecular Biology Institute, University of California, Los Angeles, CA, USA.
Stephen YoungMolecular Biology Institute, University of California, Los Angeles, CA, USA.
Amander T ClarkDepartment of Molecular Cell and Developmental Biology, University of California, Los Angeles, CA, USA.
Dino Di CarloDepartment of Bioengineering, University of California, Los Angeles, CA, USA.
University of California, Los Angeles · USCalifornia NanoSystems Institute · USBroad Center · US

Funding

Understanding Epigenetic Remodeling in Primordial Germ CellsR01HD058047 · NICHD · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI CLARK, AMANDER · 2009 to 2023
$5.6M
NICHD NIH HHS R01 HD058047
6 · The paper itself

Abstract

We introduce a label-free method to rapidly phenotype and classify cells purely based on physical properties. We extract 15 biophysical parameters from cells as they deform in a microfluidic stretching flow field via high-speed microscopy and apply machine-learning approaches to discriminate different cell types and states. When employing the full 15 dimensional dataset, the technique robustly classifies individual cells based on their pluripotency, with accuracy above 95%. Rheological and morphological properties of cells while deforming were critical for this classification. We also show the application of this method in accurate classifying cells based on their viability, drug screening and detecting populations of malignant cells in mixed samples. We show that some of the extracted parameters are not linearly independent, and in fact we reach maximum classification accuracy by using only a subset of parameters. However, the informative subsets could vary depending on cell types in the sample. This work shows the utility of an assay purely based on intrinsic biophysical properties of cells to identify changes in cell state. In addition to a label-free alternative to flow cytometry in certain applications, this work, also can provide novel intracellular metrics that would not be feasible with labeled approaches (i.e. flow cytometry).

Indexed as

Flow CytometryMachine LearningAnimalsBiophysicsCell CountEmbryonic Stem CellsFibroblastsHumansHydrodynamicsMiceMicrofluidic Analytical TechniquesMicrofluidicsPhenotypeRheology

Identifiers

PMID27910869
PMCPMC5133672
OpenAlexW2558750038

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.