Evidence map›Paper›PMID 40994932›Full record

ArticlePhotonics research2025

High area and volumetric throughput parallel two-photon fluorescence microscopy using silicon photomultiplier arrays.

Vincent D Ching-Roa, Chi Z Huang, Michael G Giacomelli

Abstract read
In one paragraph

Article in Photonics research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

3 authors.

Vincent D Ching-RoaDepartment of Biomedical Engineering, University of Rochester, Rochester, New York 14627, USA.ORCID 0000-0003-3836-534X
Chi Z HuangDepartment of Biomedical Engineering, University of Rochester, Rochester, New York 14627, USA.ORCID 0009-0002-5555-1232
Michael G GiacomelliDepartment of Biomedical Engineering, University of Rochester, Rochester, New York 14627, USA.ORCID 0000-0002-2570-0770

Funding

Two photon fluorescence microscopy for dermatologic surgery and biopsyR37CA258376 · NCI · UNIVERSITY OF ROCHESTER · PI Michael Gene Giacomelli · 2021 to 2026
$2.0M
Two photon microscopy and optical clearing for volumetric imaging of melanoma surgical marginsR21EB032839 · NIBIB · UNIVERSITY OF ROCHESTER · PI GIACOMELLI, MICHAEL GENE · 2022 to 2023
$364k
NCI NIH HHS R37 CA258376NIBIB NIH HHS R21 EB032839
6 · The paper itself

Abstract

Two-photon fluorescence microscopy (TPFM) is widely used for imaging of biological tissue due to its robustness to scattering, high resolution, and ease of multiplexing fluorescent probes. However, TPFM volumetric imaging rates are typically low, limiting the ability to image whole cleared tissues and large surgical specimens. While innovations in TPFM technology, such as parallel-scanning, have drastically increased imaging speed, these improvements have typically focused on high frame rate, single field-of-view imaging rather than extending the area/volume imaging rate. In this work, we bridge the gap between high imaging speed and high area and volumetric imaging throughput by combining parallel scanning with tilted-plane strip-scanning using custom silicon photomultiplier (SiPM) tiled-array detectors. We demonstrate 200 MP/s with four spectral channels (800 MSpectra/s) and an effective area imaging speed of up to 52 mm

Identifiers

PMID40994932
PMCPMC12456228

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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.