Evidence map›Paper›PMID 42814809›Full record

ArticleScience advances2026

A computational super-resolution framework for multidimensional fluorescence imaging.

Wonsang Hwang, Bingying Zhao, Kai Guo, Jenu V Chacko, Sinyoung Jeong, Adán Guerrero, Jerome Mertz, Conor L Evans, Iván Coto Hernández

Abstract read
In one paragraph

Article in Science advances, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

9 authors.

Wonsang HwangWellman Center for Photomedicine, Harvard Medical School, Massachusetts General Hospital, CNY149, 13th St, Charlestown, MA 02129, USA.ORCID 0000-0002-6156-9554
Bingying ZhaoDepartment of Electrical and Computer Engineering, Boston University, 8 St Mary's St, Boston, MA 02215, USA.ORCID 0009-0003-5208-5317
Kai GuoCollege of Graduate and Professional Studies, Trine University, 999 Republic Dr Suite 200, Allen Park, Detroit, MI 48101, USA.
Jenu V ChackoLaboratory for Optical and Computational Instrumentation, University of Wisconsin-Madison, Madison, WI 53706, USA.ORCID 0000-0002-6676-0358
Sinyoung JeongIntek Scientific, 1 Broadway, Cambridge, MA 02142, USA.ORCID 0000-0001-9407-7006
Adán GuerreroLaboratorio Nacional de Microscopía Avanzada, Instituto de Biotecnología, Universidad Nacional Autónoma de México, Cuernavaca, Morelos, Mexico.ORCID 0000-0002-4389-5516
Jerome MertzDepartment of Biomedical Engineering, Boston University, 44 Cummington Mall, Boston, MA 02215, USA.ORCID 0000-0002-6343-9155
Conor L EvansWellman Center for Photomedicine, Harvard Medical School, Massachusetts General Hospital, CNY149, 13th St, Charlestown, MA 02129, USA.ORCID 0000-0003-2185-6505
Iván Coto HernándezCenter for Interdisciplinary Innovation in Imaging, Massachusetts General Hospital and Harvard Medical School, 149 13th St, Charlestown, MA 02129, USA.ORCID 0000-0003-3611-7959

Funding

Super-resolved multiphoton microscopy with dual output ultrafast laserK25EB032864 · NIBIB · MASSACHUSETTS GENERAL HOSPITAL · PI COTO HERNANDEZ, IVAN · 2023 to 2025
$436k
NIBIB NIH HHS K25 EB032864
6 · The paper itself

Abstract

Fully capturing the heterogeneity of biological processes remains a central challenge, as conventional confocal microscopy typically surveys large ensembles of molecules within a small volume. The development of super-resolution imaging enables the capture of images with exceptional detail. When super-resolution is combined with functional imaging, such as fluorescence lifetime and spectral imaging, it provides better separation of image constituents and sensing of environmental properties at the nanoscale. These multidimensional imaging approaches often acquire functional and fluorescence images separately and then merge the resulting datasets, a post hoc approach that risks dynamic range mismatches and the loss of subtle molecular signals. Here, we introduce a computational super-resolution framework based on the deblurring by pixel reassignment (DPR) algorithm, which processes multidimensional data as high-dimensional tensors, integrating spatial axes with fluorescence lifetime or spectral information into a single dataset. Using DPR, high-resolution details can be extracted from conventional fluorescence microscopy images, even from a single capture. We show that this approach enhances the spatial resolution of multidimensional datasets without compromising quantitative fidelity. As a proof of concept, we demonstrate super-resolution multimodal imaging (intensity, lifetime, and spectra), revealing fine-scale details while preserving signals from rare or low-intensity molecular events. This accessible yet powerful method paves the way for quantitative, single-molecule-level insights into complex biological systems.

Identifiers

PMID42814809
PMCPMC13626035

What OpenQuestion holds

Textmetadata
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.