Evidence map›Paper›PMID 39139100›Full record

ArticleGenetics2024

Automated cell lineage reconstruction using label-free 4D microscopy.

Matthew Waliman, Ryan L Johnson, Gunalan Natesan, Neil A Peinado, Shiqin Tan, Anthony Santella, Ray L Hong, Pavak K Shah

Abstract read
In one paragraph

Article in Genetics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Cell lineage tracing: Methods, applications, and challenges.Quantitative biology (Beijing, China) · 2025
    Review
  2. Article
  3. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors.

Matthew WalimanDepartment of Electrical and Computer Engineering, University of California, Los Angeles, Los Angeles, CA 90095, USA.
Ryan L JohnsonDepartment of Molecular, Cell and Developmental Biology, University of California, Los Angeles, Los Angeles, CA 90095, USA.
Gunalan NatesanDepartment of Molecular, Cell and Developmental Biology, University of California, Los Angeles, Los Angeles, CA 90095, USA.
Neil A PeinadoDepartment of Molecular, Cell and Developmental Biology, University of California, Los Angeles, Los Angeles, CA 90095, USA.ORCID 0000-0002-1231-5339
Shiqin TanDepartment of Computational and Systems Biology, University of California, Los Angeles, Los Angeles, CA 90095, USA.
Anthony SantellaMolecular Cytology Core, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA.
Ray L HongDepartment of Biology, California State University, Northridge, Northridge, CA 91325, USA.ORCID 0000-0003-1870-8659
Pavak K ShahDepartment of Molecular, Cell and Developmental Biology, University of California, Los Angeles, Los Angeles, CA 90095, USA.ORCID 0000-0002-2603-5995

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Hongbiao Carl Lekaye · 1985 to 2026
$347.4M
Enhancing and expanding the CGC Strain CollectionP40OD010440 · OD · UNIVERSITY OF MINNESOTA · PI Ann E. Rougvie · 2012 to 2026
$7.5M
Research Training in Cell and Molecular BiologyT32GM145388 · NIGMS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI Jorge Torres · 2022 to 2026
$5.2M
Cell lineage-based investigation of chemosensory neuron developmentR21DC019485 · NIDCD · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI SHAH, PAVAK KIRIT · 2022 to 2023
$428k
NCI NIH HHS P30 CA008748NIDCD NIH HHS R21 DC019485NIGMS NIH HHS T32 GM145388NIH HHS P40 OD010440NIH HHS R21DC019485
6 · The paper itself

Abstract

Patterns of lineal descent play a critical role in the development of metazoan embryos. In eutelic organisms that generate a fixed number of somatic cells, invariance in the topology of their cell lineage provides a powerful opportunity to interrogate developmental events with empirical repeatability across individuals. Studies of embryonic development using the nematode Caenorhabditis elegans have been drivers of discovery. These studies have depended heavily on high-throughput lineage tracing enabled by 4D fluorescence microscopy and robust computer vision pipelines. For a range of applications, computer-aided yet manual lineage tracing using 4D label-free microscopy remains an essential tool. Deep learning approaches to cell detection and tracking in fluorescence microscopy have advanced significantly in recent years, yet solutions for automating cell detection and tracking in 3D label-free imaging of dense tissues and embryos remain inaccessible. Here, we describe embGAN, a deep learning pipeline that addresses the challenge of automated cell detection and tracking in label-free 3D time-lapse imaging. embGAN requires no manual data annotation for training, learns robust detections that exhibits a high degree of scale invariance, and generalizes well to images acquired in multiple labs on multiple instruments. We characterize embGAN's performance using lineage tracing in the C. elegans embryo as a benchmark. embGAN achieves near-state-of-the-art performance in cell detection and tracking, enabling high-throughput studies of cell lineage without the need for fluorescent reporters or transgenics.

Indexed as

Caenorhabditis elegansCell LineageAnimalsCell TrackingDeep LearningImage Processing, Computer-AssistedImaging, Three-DimensionalMicroscopy, Fluorescencecell lineagedevelopmentimage analysisnematode

Identifiers

PMID39139100
PMCPMC11457935

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.