Virtual Slice Imaging

Virtual slice imaging is a computational technique that generates two-dimensional views from three-dimensional biological imaging data, allowing researchers to examine internal structures without physically sectioning a specimen. The method uses volumetric datasets and digital reconstruction to extract virtual sections at selected depths or orientations, preserving spatial relationships within tissues and organs. In biology, virtual slice imaging supports the analysis of anatomy, cellular organization, development, and disease-related changes while reducing sample damage and enabling repeated examination of the same specimen. It also facilitates quantitative measurements, image comparison, and integration with other three-dimensional imaging and modeling approaches.

Virtual Slice Imaging - Related Videos

Research

JoVE Journal - Behavior

Two-photon Calcium Imaging in Mice Navigating a Virtual Reality Environment

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Cited by 98 •

2014

Here we describe the experimental procedures involved in two-photon imaging of mouse cortex during behavior in a virtual reality environment.

Brain Imaging Investigation of the Neural Correlates of Observing Virtual Social Interactions

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Cited by 10 •

2011

This article demonstrates an experimental design in which whole-body animated characters are used in conjunction with functional magnetic resonance imaging (fMRI) to investigate the neural correlates of observing virtual social interactions.

Preparation of Acute Subventricular Zone Slices for Calcium Imaging

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Cited by 2 •

2012

A method to load subventricular zone (SVZ) cells with calcium indicator dyes for recording calcium activity is described. The postnatal SVZ contains tightly packed cells including neural progenitor cells and neuroblasts. Rather than using bath loading we injected the dye by pressure inside the tissue allowing better dye diffusion.

Ex Vivo Culture and Imaging of Oculomotor Slices from Transgenic Mouse Embryos

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2025

This video demonstrates the ex vivo culture and imaging of oculomotor slices from transgenic mouse embryos. The embryos are isolated and embedded in agarose. Using a vibratome, slices containing the oculomotor nuclei and eyes are obtained. The slices are maintained in culture and imaged using a fluorescence microscope.

A Rapid Approach to High-Resolution Fluorescence Imaging in Semi-Thick Brain Slices

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Cited by 10 •

2011

Here we describe a rapid and simple method to image fluorescently labeled cells in semi-thick brain slices. By fixing, slicing, and optically clearing brain tissue we describe how standard epifluorescent or confocal imaging can be used to visualize individual cells and neuronal networks within intact nervous tissue.

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