Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Experiment Videos

PreMosa: extracting 2D surfaces from 3D microscopy mosaics.

Corinna Blasse1, Stephan Saalfeld2, Raphaël Etournay1,3

  • 1Max Planck Institute of Molecular Cell Biology and Genetics, Dresden 01307, Germany.

Bioinformatics (Oxford, England)
|April 7, 2017
PubMed
Summary
This summary is machine-generated.

Related Concept Videos

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

The Vertebrate Genomes Project Phase I: A global reference genome resource.

bioRxiv : the preprint server for biology·2026
Same author

Complete sequencing of medaka genomes reveals the architecture of centromeric satellites, giant mobile elements, and sex chromosomes.

Genome research·2026
Same author

The genome sequence of <i>Saccopteryx leptura, Schreber, 1774</i> (Chiroptera, Emballonuridae, Saccopteryx).

Wellcome open research·2026
Same author

Evidence for chronological diversification of spinal neuron subtypes by a shared sequence of transcription factors.

Science advances·2026
Same author

Sexual dimorphism in the complete connectome of the <i>Drosophila</i> male central nervous system.

bioRxiv : the preprint server for biology·2025
Same author

Evaluation of sequencing reads at scale using rdeval.

Bioinformatics (Oxford, England)·2025

PreMosa is a new automated pipeline that preprocesses microscopy images of epithelial tissues. It efficiently extracts, maps, and stitches stained cell junctions into a single, high-contrast 2D image for easier analysis.

Area of Science:

  • Biological imaging
  • Cell biology
  • Tissue engineering

Background:

  • Understanding tissue development, organization, and function is crucial in biology.
  • Epithelial tissues with fluorescently labeled adherence junctions are a key research area.
  • Microscopy requires collecting large mosaics of 3D stacks for tissue analysis.

Purpose of the Study:

  • To develop an efficient, automated pipeline for preprocessing large-scale microscopy datasets of epithelial tissues.
  • To simplify downstream interpretation of complex biological images.
  • To generate a single, high-contrast 2D image from multiple 3D stacks.

Main Methods:

  • Developed PreMosa, a four-step automated preprocessing pipeline.
  • Implemented a novel algorithm for 2D projection based on contrast, intensity, and smoothness maximization.

Related Experiment Videos

  • Utilized a mosaic melding algorithm for global contrast adjustment and seamless stitching.
  • Performed evaluations using ground-truth datasets and real biological samples.
  • Main Results:

    • PreMosa successfully generates a single 2D image of the stained manifold with optimized contrast and even illumination.
    • The 2D projection algorithm accurately identifies and maps the tissue manifold.
    • The mosaic melding algorithm produces seamless, high-contrast composite images.
    • The pipeline demonstrated effectiveness on Drosophila melanogaster wings and Schmidtae mediterranea datasets.

    Conclusions:

    • PreMosa offers an efficient and automated solution for preprocessing complex biological image data.
    • The pipeline significantly simplifies the analysis of large-scale tissue imaging datasets.
    • PreMosa facilitates deeper insights into tissue development, organization, and function.