Evidence map›Paper›PMID 39804144›Full record

ArticleBriefings in bioinformatics2024

A framework of multi-view machine learning for biological spectral unmixing of fluorophores with overlapping excitation and emission spectra.

Ruogu Wang, Yunlong Feng, Alex M Valm

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

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0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

3 authors.

Ruogu WangDepartment of Biology, University at Albany, SUNY, 1400 Washington Ave, Albany, NY 12222, United States.
Yunlong FengDepartment of Mathematics and Statistics, University at Albany, SUNY, 1400 Washington Ave, Albany, NY 12222, United States.
Alex M ValmDepartment of Biology, University at Albany, SUNY, 1400 Washington Ave, Albany, NY 12222, United States.

Funding

Biofilm Spatial Structure in the Transition from Health to Periodontal DiseaseR01DE031213 · NIDCR · STATE UNIVERSITY OF NEW YORK AT ALBANY · PI Alex M Valm · 2022 to 2026
$2.3M
Oral microbial community structure and assembly: from molecule to microbiomeR01DE030927 · NIDCR · STATE UNIVERSITY OF NEW YORK AT ALBANY · PI VALM, ALEX M · 2021 to 2025
$1.8M
Zeiss LSM 980 Confocal Microscope SystemS10OD028600 · OD · STATE UNIVERSITY OF NEW YORK AT ALBANY · PI VALM, ALEX M · 2022 to 2022
$477k
National Science Foundation 1636933NIDCR NIH HHS R01 DE030927NIDCR NIH HHS R01 DE031213NIH HHS R01DE031213NIH HHS S10 OD028600
6 · The paper itself

Abstract

The accuracy of assigning fluorophore identity and abundance, known as spectral unmixing, in biological fluorescence microscopy images remains a significant challenge due to the substantial overlap in emission spectra among fluorophores. In traditional laser scanning confocal spectral microscopy, fluorophore information is acquired by recording emission spectra with a single combination of discrete excitation wavelengths. However, organic fluorophores possess characteristic excitation spectra in addition to their unique emission spectral signatures. In this paper, we propose a generalized multi-view machine learning approach that leverages both excitation and emission spectra to significantly improve the accuracy in differentiating multiple highly overlapping fluorophores in a single image. By recording emission spectra of the same field with multiple combinations of excitation wavelengths, we obtain data representing different views of the underlying fluorophore distribution in the sample. We then propose a multi-view machine learning framework that allows for the flexible incorporation of noise information and abundance constraints, enabling the extraction of spectral signatures from reference images and efficient recovery of corresponding abundances in unknown mixed images. Numerical experiments on simulated image data demonstrate the method's efficacy in improving accuracy, allowing for the discrimination of 100 fluorophores with highly overlapping spectra. Furthermore, validation on images of mixtures of fluorescently labeled Escherichia coli highlights the power of the proposed multi-view strategy in discriminating fluorophores with spectral overlap in real biological images.

Indexed as

Fluorescent DyesImage Processing, Computer-AssistedMachine LearningAlgorithmsMicroscopy, ConfocalMicroscopy, FluorescenceFluorescent Dyesbiological spectral unmixingfluorescence imagingmulti-view machine learningspectral overlap

Identifiers

PMID39804144
PMCPMC11726699

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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.