Detail of Membrane



Project
SSBD:Repository
Title
Time-lapse microscopy images of cellular dynamics of a C. elegans embryo
Description
NA
Release, Updated
2017-03-01,
2017-11-15
License
CC BY-NC-SA
Kind
Image data based on Experiment
File Formats
Data size
19.8 MB

Organism
C. elegans ( NCBI:txid6239 )
Strain(s)
-
Cell Line
-
Protein names
PTEN

Datatype
cellular dynamics
Molecular Function (MF)
Biological Process (BP)
embryo development ( GO:0009790 )
Cellular Component (CC)
membrane ( GO:0016020 )
Biological Imaging Method
XYZ Scale
XY: 0.444 micrometer/pixel, Z: 0.500 micrometer/frame
T scale
-

Image Acquisition
Experiment type
TimeLapse
Microscope type
ConfocalMicroscope
Acquisition mode
Other
Contrast method
Other
Microscope model
-
Detector model
-
Objective model
-
Filter set
-

Summary of Methods
See details in Azuma & Onami et al. (2017) BMC Bioinformatics, 18(1): 307.
Related paper(s)

Yusuke Azuma, Shuichi Onami (2017) Biologically constrained optimization based cell membrane segmentation in C. elegans embryos., BMC bioinformatics, Volume 18, Number 1, pp. 307

Published in 2017 Jun 19 (Electronic publication in June 19, 2017, midnight )

(Abstract) BACKGROUND: Recent advances in bioimaging and automated analysis methods have enabled the large-scale systematic analysis of cellular dynamics during the embryonic development of Caenorhabditis elegans. Most of these analyses have focused on cell lineage tracing rather than cell shape dynamics. Cell shape analysis requires cell membrane segmentation, which is challenging because of insufficient resolution and image quality. This problem is currently solved by complicated segmentation methods requiring laborious and time consuming parameter adjustments. RESULTS: Our new framework BCOMS (Biologically Constrained Optimization based cell Membrane Segmentation) automates the extraction of the cell shape of C. elegans embryos. Both the segmentation and evaluation processes are automated. To automate the evaluation, we solve an optimization problem under biological constraints. The performance of BCOMS was validated against a manually created ground truth of the 24-cell stage embryo. The average deviation of 25 cell shape features was 5.6%. The deviation was mainly caused by membranes parallel to the focal planes, which either contact the surfaces of adjacent cells or make no contact with other cells. Because segmentation of these membranes was difficult even by manual inspection, the automated segmentation was sufficiently accurate for cell shape analysis. As the number of manually created ground truths is necessarily limited, we compared the segmentation results between two adjacent time points. Across all cells and all cell cycles, the average deviation of the 25 cell shape features was 4.3%, smaller than that between the automated segmentation result and ground truth. CONCLUSIONS: BCOMS automated the accurate extraction of cell shapes in developing C. elegans embryos. By replacing image processing parameters with easily adjustable biological constraints, BCOMS provides a user-friendly framework. The framework is also applicable to other model organisms. Creating the biological constraints is a critical step requiring collaboration between an experimentalist and a software developer.
(MeSH Terms)

Contact
Shuichi Onami , RIKEN , Quantitative Biology Center , Laboratory for Developmental Dynamics
Contributors
Yusuke Azuma, Shuichi Onami

OMERO Dataset
OMERO Project
Source