Automatic Segmentation of Intravital Fluorescence Microscopy Images by K-Means Clustering of FLIM Phasors.

Article

Abstract

Fluorescence lifetime imaging microscopy (FLIM) provides additional contrast for fluorophores with overlapping emission spectra. The phasor approach to FLIM greatly reduces the complexity of FLIM analysis and enables a useful image segmentation technique by selecting adjacent phasor points and labeling their corresponding pixels with different colors. This phasor labeling process, however, is empirical and could lead to biased results. In this Letter, we present a novel and unbiased approach to automate the phasor labeling process using an unsupervised machine learning technique, i.e., K-means clustering. In addition, we provide an open-source, user-friendly program that enables users to easily employ the proposed approach. We demonstrate successful image segmentation on 2D and 3D FLIM images of fixed cells and living animals acquired with two different FLIM systems. Finally, we evaluate how different parameters affect the segmentation result and provide a guideline for users to achieve optimal performance.

Attributes

Attribute NameValues
Creator
  • Yide Zhang

  • Takashi Hato

  • Pierre Dagher

  • Evan Nichols

  • Cody Smith

  • Kenneth Dunn

  • Scott Howard

Journal or Work Title
  • Optics Letters

Volume
  • 44

Issue
  • 16

First Page
  • 3928

ISSN
  • 0146-9592

Publication Date
  • 2019-08

Subject
  • Nikon A1R

Publisher
  • Optical Society of America

Date Created
  • 2020-04-08

Language
  • English

Departments and Units
Record Visibility Public
Content License
  • All rights reserved

Digital Object Identifier

doi:10.1364/ol.44.003928

This DOI is the best way to cite this article.