Evidence map›Paper›PMID 35573197›Full record

ArticleiScience2022

New open-source software for subcellular segmentation and analysis of spatiotemporal fluorescence signals using deep learning.

Sharif Amit Kamran, Khondker Fariha Hossain, Hussein Moghnieh, Sarah Riar, Allison Bartlett, Alireza Tavakkoli, Kenton M Sanders, Salah A Baker

Abstract read
In one paragraph

Article in iScience, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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

12 citing papers in PubMed.

  1. Article
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  7. CaPhysiological reviews · 2024
    Review
  8. Live-cell imaging in the deep learning era.Current opinion in cell biology · 2023
    Review
  9. Article
  10. Review
  11. Article
  12. Article
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

8 authors.

Sharif Amit KamranDepartment of Physiology and Cell Biology, University of Nevada, Reno School of Medicine, Anderson Medical Building MS352, Reno, NV 89557, USA.
Khondker Fariha HossainDepartment of Computer Science and Engineering, University of Nevada, Reno, NV 89557, USA.
Hussein MoghniehDepartment of Electrical and Computer Engineering], McGill University, Montréal, QC H3A 0E9, Canada.
Sarah RiarDepartment of Physiology and Cell Biology, University of Nevada, Reno School of Medicine, Anderson Medical Building MS352, Reno, NV 89557, USA.
Allison BartlettDepartment of Physiology and Cell Biology, University of Nevada, Reno School of Medicine, Anderson Medical Building MS352, Reno, NV 89557, USA.
Alireza TavakkoliDepartment of Computer Science and Engineering, University of Nevada, Reno, NV 89557, USA.
Kenton M SandersDepartment of Physiology and Cell Biology, University of Nevada, Reno School of Medicine, Anderson Medical Building MS352, Reno, NV 89557, USA.
Salah A BakerDepartment of Physiology and Cell Biology, University of Nevada, Reno School of Medicine, Anderson Medical Building MS352, Reno, NV 89557, USA.

Funding

Role of interstitial cells of Cajal in patterned colonic motor activityR01DK120759 · NIDDK · UNIVERSITY OF NEVADA RENO · PI Sal Baker, KENTON M SANDERS · 2019 to 2026
$3.4M
NIDDK NIH HHS R01 DK120759
6 · The paper itself

Abstract

Cellular imaging instrumentation advancements as well as readily available optogenetic and fluorescence sensors have yielded a profound need for fast, accurate, and standardized analysis. Deep-learning architectures have revolutionized the field of biomedical image analysis and have achieved state-of-the-art accuracy. Despite these advancements, deep learning architectures for the segmentation of subcellular fluorescence signals is lacking. Cellular dynamic fluorescence signals can be plotted and visualized using spatiotemporal maps (STMaps), and currently their segmentation and quantification are hindered by slow workflow speed and lack of accuracy, especially for large datasets. In this study, we provide a software tool that utilizes a deep-learning methodology to fundamentally overcome signal segmentation challenges. The software framework demonstrates highly optimized and accurate calcium signal segmentation and provides a fast analysis pipeline that can accommodate different patterns of signals across multiple cell types. The software allows seamless data accessibility, quantification, and graphical visualization and enables large dataset analysis throughput.

Indexed as

Artificial intelligenceAutomation in bioinformaticsBioinformaticsCell biology

Identifiers

PMID35573197
PMCPMC9095751

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.