Evidence map›Paper›PMID 37521315›Full record

ArticleFrontiers in bioinformatics2023

Machine learning enhanced cell tracking.

Christopher J Soelistyo, Kristina Ulicna, Alan R Lowe

Open access · goldAbstract read
In one paragraph

Article in Frontiers in bioinformatics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
5.4field-weighted citation impact, top 5% 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

9 citing papers in PubMed, 15 citations in OpenAlex.

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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

3 authors at 2 institutions in 1 country.

Christopher J SoelistyoDepartment of Structural and Molecular Biology, University College London, London, United Kingdom.
Kristina UlicnaDepartment of Structural and Molecular Biology, University College London, London, United Kingdom.
Alan R LoweDepartment of Structural and Molecular Biology, University College London, London, United Kingdom.
University College London · GBInstitute of Structural and Molecular Biology · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Quantifying cell biology in space and time requires computational methods to detect cells, measure their properties, and assemble these into meaningful trajectories. In this aspect, machine learning (ML) is having a transformational effect on bioimage analysis, now enabling robust cell detection in multidimensional image data. However, the task of cell tracking, or constructing accurate multi-generational lineages from imaging data, remains an open challenge. Most cell tracking algorithms are largely based on our prior knowledge of cell behaviors, and as such, are difficult to generalize to new and unseen cell types or datasets. Here, we propose that ML provides the framework to learn aspects of cell behavior using cell tracking as the task to be learned. We suggest that advances in representation learning, cell tracking datasets, metrics, and methods for constructing and evaluating tracking solutions can all form part of an end-to-end ML-enhanced pipeline. These developments will lead the way to new computational methods that can be used to understand complex, time-evolving biological systems.

Indexed as

bioimage analysiscell trackingcomputer visionmachine learning (ML)optimisationtracking

Identifiers

PMID37521315
PMCPMC10380934
OpenAlexW4384406485

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.