Abstract

BackgroundRecent advances in tissue clearing techniques, combined with high-speed image acquisition through light sheet microscopy, enable rapid three-dimensional (3D) imaging of biological specimens, such as whole mouse brains, in a matter of hours. Quantitative analysis of such 3D images can help us understand how changes in brain structure lead to differences in behavior or cognition, but distinguishing densely packed features of interest, such as nuclei, from background can be challenging. Recent deep learning-based nuclear segmentation algorithms show great promise for automated segmentation, but require large numbers of accurate manually labeled nuclei as training data.ResultsWe present Segmentor, an open-source tool for reliable, efficient, and user-friendly manual annotation and refinement of objects (e.g., nuclei) within 3D light sheet microscopy images. Segmentor employs a hybrid 2D-3D approach for visualizing and segmenting objects and contains features for automatic region splitting, designed specifically for streamlining the process of 3D segmentation of nuclei. We show that editing simultaneously in 2D and 3D using Segmentor significantly decreases time spent on manual annotations without affecting accuracy as compared to editing the same set of images with only 2D capabilities.ConclusionsSegmentor is a tool for increased efficiency of manual annotation and refinement of 3D objects that can be used to train deep learning segmentation algorithms, and is available at https://www.nucleininja.org/ and https://github.com/RENCI/Segmentor.

Highlights

  • Recent advances in tissue clearing techniques, combined with highspeed image acquisition through light sheet microscopy, enable rapid three-dimen‐ sional (3D) imaging of biological specimens, such as whole mouse brains, in a matter of hours

  • Combined with high-speed image acquisition through light sheet microscopy, the full 3D extent of adult mouse brain specimens can be imaged at micron resolution in a matter of hours [4,5,6,7]

  • We focused on implementing features that enhance the efficiency of this task, including synchronized 2D + 3D visualization and editing, intuitive visibility controls, and semi-automated correction of segmentation errors common to light sheet microscopy of brain tissue

Read more

Summary

Introduction

Recent advances in tissue clearing techniques, combined with highspeed image acquisition through light sheet microscopy, enable rapid three-dimen‐ sional (3D) imaging of biological specimens, such as whole mouse brains, in a matter of hours. Quantitative analysis of such 3D images can help us understand how changes in brain structure lead to differences in behavior or cognition, but distinguishing densely packed features of interest, such as nuclei, from background can be challeng‐ ing. Combined with high-speed image acquisition through light sheet microscopy, the full 3D extent of adult mouse brain specimens can be imaged at micron resolution in a matter of hours [4,5,6,7]

Objectives
Results
Discussion
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call