Evidence map›Paper›PMID 38050354›Full record

ArticleBiophysical journal2024

Deep learning reduces data requirements and allows real-time measurements in imaging FCS.

Wai Hoh Tang, Shao Ren Sim, Daniel Ying Kia Aik, Ashwin Venkata Subba Nelanuthala, Thamarailingam Athilingam, Adrian Röllin, Thorsten Wohland

Abstract read
In one paragraph

Article in Biophysical journal, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 citing papers in PubMed.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors.

Wai Hoh TangDepartment of Biological Sciences, National University of Singapore, Singapore, Singapore; NUS Centre for Bio-Imaging Sciences, National University of Singapore, Singapore, Singapore; Department of Statistics and Data Science, National University of Singapore, Singapore, Singapore; Institute of Digital Molecular Analytics and Science, National University of Singapore, Singapore, Singapore.
Shao Ren SimDepartment of Biological Sciences, National University of Singapore, Singapore, Singapore; NUS Centre for Bio-Imaging Sciences, National University of Singapore, Singapore, Singapore.
Daniel Ying Kia AikDepartment of Biological Sciences, National University of Singapore, Singapore, Singapore; NUS Centre for Bio-Imaging Sciences, National University of Singapore, Singapore, Singapore; Institute of Digital Molecular Analytics and Science, National University of Singapore, Singapore, Singapore; Department of Chemistry, National University of Singapore, Singapore, Singapore.
Ashwin Venkata Subba NelanuthalaDepartment of Biological Sciences, National University of Singapore, Singapore, Singapore; NUS Centre for Bio-Imaging Sciences, National University of Singapore, Singapore, Singapore.
Thamarailingam AthilingamMechanobiology Institute, National University of Singapore, Singapore, Singapore.
Adrian RöllinDepartment of Statistics and Data Science, National University of Singapore, Singapore, Singapore.
Thorsten WohlandDepartment of Biological Sciences, National University of Singapore, Singapore, Singapore; NUS Centre for Bio-Imaging Sciences, National University of Singapore, Singapore, Singapore; Institute of Digital Molecular Analytics and Science, National University of Singapore, Singapore, Singapore; Department of Chemistry, National University of Singapore, Singapore, Singapore. Electronic address: twohland@nus.edu.sg.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Imaging fluorescence correlation spectroscopy (FCS) is a powerful tool to extract information on molecular mobilities, actions, and interactions in live cells, tissues, and organisms. Nevertheless, several limitations restrict its applicability. First, FCS is data hungry, requiring 50,000 frames at 1-ms time resolution to obtain accurate parameter estimates. Second, the data size makes evaluation slow. Third, as FCS evaluation is model dependent, data evaluation is significantly slowed unless analytic models are available. Here, we introduce two convolutional neural networks-FCSNet and ImFCSNet-for correlation and intensity trace analysis, respectively. FCSNet robustly predicts parameters in 2D and 3D live samples. ImFCSNet reduces the amount of data required for accurate parameter retrieval by at least one order of magnitude and makes correct estimates even in moderately defocused samples. Both convolutional neural networks are trained on simulated data, are model agnostic, and allow autonomous, real-time evaluation of imaging FCS measurements.

Indexed as

Deep LearningSpectrometry, Fluorescence

Identifiers

PMID38050354
PMCPMC10995408

What OpenQuestion holds

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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.