Evidence map›Paper›PMID 32282792›Full record

ArticlePLoS computational biology2020

DeLTA: Automated cell segmentation, tracking, and lineage reconstruction using deep learning.

Jean-Baptiste Lugagne, Haonan Lin, Mary J Dunlop

Abstract read
In one paragraph

Article in PLoS computational biology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 92 papers.

0numbers the graph read from it
0cells of the map it votes in
92citing 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

92 citing papers in PubMed.

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  14. Unique growth and morphology properties of Clade 5bioRxiv : the preprint server for biology · 2025
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  17. Colony pattern multistability emerges from a bistable switch.Proceedings of the National Academy of Sciences of the United States of America · 2025
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32 more citing papers are in PubMed but not listed here.

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.

Jean-Baptiste LugagneDepartment of Biomedical Engineering, Boston University, Boston, Massachussets, United States of America.ORCID 0000-0002-8374-6590
Haonan LinDepartment of Biomedical Engineering, Boston University, Boston, Massachussets, United States of America.ORCID 0000-0003-0437-5902
Mary J DunlopDepartment of Biomedical Engineering, Boston University, Boston, Massachussets, United States of America.ORCID 0000-0002-9261-8216

Funding

Feedback and Noise in a Multiple Antibiotic Resistance CircuitR01AI102922 · NIAID · UNIVERSITY OF VERMONT & ST AGRIC COLLEGE · PI Mary J. Dunlop · 2014 to 2026
$4.7M
Efflux pumps and the emergence of antibiotic resistance in single cellsR21AI137843 · NIAID · BOSTON UNIVERSITY (CHARLES RIVER CAMPUS) · PI DUNLOP, MARY · 2018 to 2019
$453k
NIAID NIH HHS R01 AI102922NIAID NIH HHS R21 AI137843
6 · The paper itself

Abstract

Microscopy image analysis is a major bottleneck in quantification of single-cell microscopy data, typically requiring human oversight and curation, which limit both accuracy and throughput. To address this, we developed a deep learning-based image analysis pipeline that performs segmentation, tracking, and lineage reconstruction. Our analysis focuses on time-lapse movies of Escherichia coli cells trapped in a "mother machine" microfluidic device, a scalable platform for long-term single-cell analysis that is widely used in the field. While deep learning has been applied to cell segmentation problems before, our approach is fundamentally innovative in that it also uses machine learning to perform cell tracking and lineage reconstruction. With this framework we are able to get high fidelity results (1% error rate), without human intervention. Further, the algorithm is fast, with complete analysis of a typical frame containing ~150 cells taking <700msec. The framework is not constrained to a particular experimental set up and has the potential to generalize to time-lapse images of other organisms or different experimental configurations. These advances open the door to a myriad of applications including real-time tracking of gene expression and high throughput analysis of strain libraries at single-cell resolution.

Indexed as

Deep LearningAlgorithmsCell TrackingComputational BiologyElectronic Data ProcessingEscherichia coliImage Processing, Computer-AssistedLab-On-A-Chip DevicesMicrofluidicsMicroscopy, FluorescenceSingle-Cell AnalysisSoftware

Identifiers

PMID32282792
PMCPMC7153852

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.