Evidence map›Paper›PMID 22947879›Full record

ArticleBiophysical journal2012

Bayesian approach to MSD-based analysis of particle motion in live cells.

Nilah Monnier, Syuan-Ming Guo, Masashi Mori, Jun He, Péter Lénárt, Mark Bathe

Open access · bronzeAbstract read
In one paragraph

Article in Biophysical journal, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 58 papers.

0numbers the graph read from it
0cells of the map it votes in
58citing papers in PubMed
9.1field-weighted citation impact, top 2% 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

58 citing papers in PubMed, 139 citations in OpenAlex.

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  13. Fluorescent nanodiamonds encapsulated byJournal of materials chemistry. B · 2021
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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

6 authors at 2 institutions in 2 countries.

Nilah MonnierDepartment of Biological Engineering, Massachusetts Institute of Technology, Cambridge, Massachusetts; Graduate Program in Biophysics, Harvard University, Cambridge, Massachusetts.
Syuan-Ming GuoDepartment of Biological Engineering, Massachusetts Institute of Technology, Cambridge, Massachusetts.
Masashi MoriCell Biology and Biophysics Unit, European Molecular Biology Laboratory, Heidelberg, Germany.
Jun HeDepartment of Biological Engineering, Massachusetts Institute of Technology, Cambridge, Massachusetts.
Péter LénártCell Biology and Biophysics Unit, European Molecular Biology Laboratory, Heidelberg, Germany.
Mark BatheDepartment of Biological Engineering, Massachusetts Institute of Technology, Cambridge, Massachusetts. Electronic address: mark.bathe@mit.edu.
Massachusetts Institute of Technology · USEuropean Molecular Biology Laboratory · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Quantitative tracking of particle motion using live-cell imaging is a powerful approach to understanding the mechanism of transport of biological molecules, organelles, and cells. However, inferring complex stochastic motion models from single-particle trajectories in an objective manner is nontrivial due to noise from sampling limitations and biological heterogeneity. Here, we present a systematic Bayesian approach to multiple-hypothesis testing of a general set of competing motion models based on particle mean-square displacements that automatically classifies particle motion, properly accounting for sampling limitations and correlated noise while appropriately penalizing model complexity according to Occam's Razor to avoid over-fitting. We test the procedure rigorously using simulated trajectories for which the underlying physical process is known, demonstrating that it chooses the simplest physical model that explains the observed data. Further, we show that computed model probabilities provide a reliability test for the downstream biological interpretation of associated parameter values. We subsequently illustrate the broad utility of the approach by applying it to disparate biological systems including experimental particle trajectories from chromosomes, kinetochores, and membrane receptors undergoing a variety of complex motions. This automated and objective Bayesian framework easily scales to large numbers of particle trajectories, making it ideal for classifying the complex motion of large numbers of single molecules and cells from high-throughput screens, as well as single-cell-, tissue-, and organism-level studies.

Indexed as

Models, BiologicalMotionBayes TheoremCell SurvivalDiffusionMovement

Identifiers

PMID22947879
PMCPMC3414897
OpenAlexW2152157469

What OpenQuestion holds

Textmetadata
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.