Evidence map›Paper›PMID 31562489›Full record

ArticleNature methods2019

Real-time volumetric microscopy of in vivo dynamics and large-scale samples with SCAPE 2.0.

Venkatakaushik Voleti, Kripa B Patel, Wenze Li, Citlali Perez Campos, Srinidhi Bharadwaj, Hang Yu, Caitlin Ford, Malte J Casper, Richard Wenwei Yan, Wenxuan Liang and 4 more

Abstract read
In one paragraph

Article in Nature methods, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 174 papers.

0numbers the graph read from it
0cells of the map it votes in
174citing 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

174 citing papers in PubMed.

  1. Article
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  9. Review
  10. Correlative Imaging Platform Linking Taste Cell Function to Molecular Identity.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Article
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  20. eLife · 2025
    Article

114 more citing papers are in PubMed but not listed here.

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

14 authors.

Venkatakaushik VoletiLaboratory for Functional Optical Imaging, Department of Biomedical Engineering, Columbia University, New York, NY, USA.
Kripa B Patel *Laboratory for Functional Optical Imaging, Department of Biomedical Engineering, Columbia University, New York, NY, USA.ORCID http://orcid.org/0000-0001-8470-714X
Wenze Li *Laboratory for Functional Optical Imaging, Department of Biomedical Engineering, Columbia University, New York, NY, USA.
Citlali Perez CamposLaboratory for Functional Optical Imaging, Department of Biomedical Engineering, Columbia University, New York, NY, USA.
Srinidhi BharadwajLaboratory for Functional Optical Imaging, Department of Biomedical Engineering, Columbia University, New York, NY, USA.ORCID http://orcid.org/0000-0002-1200-0070
Hang YuLaboratory for Functional Optical Imaging, Department of Biomedical Engineering, Columbia University, New York, NY, USA.ORCID http://orcid.org/0000-0003-2923-7872
Caitlin FordDepartment of Pediatrics, College of Physicians & Surgeons, Columbia University, New York, NY, USA.
Malte J CasperLaboratory for Functional Optical Imaging, Department of Biomedical Engineering, Columbia University, New York, NY, USA.ORCID http://orcid.org/0000-0002-6879-691X
Richard Wenwei YanLaboratory for Functional Optical Imaging, Department of Biomedical Engineering, Columbia University, New York, NY, USA.
Wenxuan LiangLaboratory for Functional Optical Imaging, Department of Biomedical Engineering, Columbia University, New York, NY, USA.
Chentao WenGraduate School of Natural Sciences, Nagoya City University, Nagoya, Japan.ORCID http://orcid.org/0000-0002-8609-476X
Koutarou D KimuraGraduate School of Natural Sciences, Nagoya City University, Nagoya, Japan.ORCID http://orcid.org/0000-0002-3359-1578
Kimara L TargoffDepartment of Pediatrics, College of Physicians & Surgeons, Columbia University, New York, NY, USA.
Elizabeth M C HillmanLaboratory for Functional Optical Imaging, Department of Biomedical Engineering, Columbia University, New York, NY, USA. Elizabeth.hillman@columbia.edu.ORCID http://orcid.org/0000-0001-5511-1451

Funding

Modeling multi-area dynamics during motor controlU19NS104649 · NINDS · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI COSTA, RUI M. · 2017 to 2021
$15.3M
Enhancing and expanding the CGC Strain CollectionP40OD010440 · OD · UNIVERSITY OF MINNESOTA · PI Ann E. Rougvie · 2012 to 2026
$7.5M
PREDOCTORAL TRAINING GRANT IN HUMAN GENETICS &DEVELOPMET32GM007088 · NIGMS · COLUMBIA UNIV NEW YORK MORNINGSIDE · PI SHEN, MICHAEL M. · 1985 to 2020
$7.1M
SCAPE microscopy for high-speed 3D imaging of cellular function in behaving animals: Continued innovation, optimization, and disseminationUF1NS108213 · NINDS · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI HILLMAN, ELIZABETH M. C. · 2018 to 2018
$3.5M
Flexible Tools for Pre-Clinical Studies to Answer Key Questions UnderlyingHeavy-Ion RadiotherapyU01CA236554 · NCI · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI BRENNER, DAVID JONATHAN, HILLMAN, ELIZABETH M. C. · 2019 to 2022
$2.6M
Mechanisms of second heart field development regulated by Nkx genesR01HL131438 · NHLBI · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI TARGOFF, KIMARA L · 2017 to 2021
$2.1M
SCAPE microscopy for high-speed in-vivo volumetric microscopy in behaving organismsU01NS094296 · NINDS · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI HILLMAN, ELIZABETH M. C. · 2015 to 2017
$2.0M
NCI NIH HHS U01 CA236554NHLBI NIH HHS R01 HL131438NIGMS NIH HHS T32 GM007088NIH HHS P40 OD010440NINDS NIH HHS U01 NS094296NINDS NIH HHS U19 NS104649NINDS NIH HHS UF1 NS108213
6 · The paper itself

Abstract

The limited per-pixel bandwidth of most microscopy methods requires compromises between field of view, sampling density and imaging speed. This limitation constrains studies involving complex motion or fast cellular signaling, and presents a major bottleneck for high-throughput structural imaging. Here, we combine high-speed intensified camera technology with a versatile, reconfigurable and dramatically improved Swept, Confocally Aligned Planar Excitation (SCAPE) microscope design that can achieve high-resolution volumetric imaging at over 300 volumes per second and over 1.2 GHz pixel rates. We demonstrate near-isotropic sampling in freely moving Caenorhabditis elegans, and analyze real-time blood flow and calcium dynamics in the beating zebrafish heart. The same system also permits high-throughput structural imaging of mounted, intact, cleared and expanded samples. SCAPE 2.0's significantly lower photodamage compared to point-scanning techniques is also confirmed. Our results demonstrate that SCAPE 2.0 is a powerful, yet accessible imaging platform for myriad emerging high-speed dynamic and high-throughput volumetric microscopy applications.

Indexed as

AnimalsCaenorhabditis elegansCalciumHeartMicroscopyPhotonsZebrafishCalcium

Identifiers

PMID31562489
PMCPMC6885017

What OpenQuestion holds

Textmetadata
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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.