ArticleBiophysical journal2019
A Jump-Distance-Based Parameter Inference Scheme for Particulate Trajectories.
Article in Biophysical journal, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 4 papers.
What it found
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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.
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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.
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Who cites it
4 citing papers in PubMed.
- Feature Selection and Hyperparameter Optimization for Machine Learned Classification of 3D Single-Particle Tracking.Chemical & biomedical imaging · 2026Article
- ThirdPeak is a flexible tool designed for the robust analysis of two- and three-dimensional tracking data.Communications biology · 2024Article
- Hop, Skip, and Jump: Hydrogen Molecular Transport through Amorphous Polyethylene Matrices Studied via Molecular Dynamics Simulations.Industrial & engineering chemistry research · 2023Article
- Impact of neurite alignment on organelle motion.Journal of the Royal Society, Interface · 2022Article
Corrections and comments
- Erratum issued
Authors and funding
2 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
This study presents an improved quantitative tool for the analysis of particulate trajectories. Particulate trajectory data appears in several different biological contexts, from the trajectory of chemotaxing bacteria to the nuclear mobility inferred from the trajectory of MS2 spots. Presently, the majority of analyses performed on particulate trajectory data have been limited to mean-squared displacement (MSD) analysis. Although simple, MSD analysis has several pitfalls, including difficulty in selecting between competing methods of motion, handling systems with multiple distinct subpopulations, and parameter extraction from limited time-series data. Here, we provide an alternative to MSD analysis using the jump distance distribution (JDD), which addresses the aforementioned issues. In particular, the method outperforms MSD analysis in the data-poor limit, thereby giving access to a larger range of temporal dynamics. In this work, we construct and validate a derivation of the JDD for different transportation modes and dimensions and implement a parameter estimation and model selection scheme. This scheme is validated, and direct improvements over MSD analysis are shown. Through an analysis of bacterial chemotaxis data, we highlight the JDD's ability to extract parameters at a variety of timescales, as well as extract underlying biological features of interest.
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Registered trials
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.