About This Project
Hyperspectral imaging could reveal biological changes without dyes or labels, offering a new window into tissue health and disease. Yet no open, biologically validated reference dataset of label-free hyperspectral signatures exists for living epithelial tissue. Using living fruit fly (Drosophila) tissue, we will compare healthy, wounded and dying states. Fluorescent validation will link each spectrum to a defined biological state, creating a calibration benchmark for the emerging field.
Ask the Scientists
Join The DiscussionWhat is the context of this research?
Hyperspectral imaging records many wavelengths at every pixel, revealing subtle differences in tissue composition and structure without dyes. Previous studies show that label-free hyperspectral imaging can distinguish living cell states and detect programmed cell death. Yet these studies use different specimens and analysis pipelines, and, to our knowledge, no shared open reference links label-free spectral signatures to independently verified states in living epithelial tissue.
The fruit fly Drosophila provides an established model for studying wound repair and patterned apoptosis under controlled conditions. We will use the wing epithelium to build a reference dataset spanning healthy, wounded and dying tissue. Our hypothesis is that wounding and apoptosis generate reproducible changes in tissue structure and composition that produce distinguishable spectral signatures, and that fluorescent markers will independently confirm the biological state represented by each spectrum.
What is the significance of this project?
What does a healthy cell look like through a hyperspectral camera? What about a wounded one, or a dying one? Surprisingly, there is no open, validated dataset to answer these basic questions.
Hyperspectral imaging is advancing rapidly, but the field lacks a critical foundation: trusted, biologically validated reference data. Without it, researchers cannot easily compare results across studies, calibrate new algorithms, or be certain that a spectral difference reflects real biology rather than experimental variation.
This project addresses that bottleneck directly. We will generate the first open reference dataset from healthy, wounded, and apoptotic Drosophila epithelial tissue, validating each state with independent fluorescent markers. The result will be a controlled, reusable benchmark that helps move hyperspectral biology from promising demonstrations toward a more rigorous, comparable, and collaborative field.
What are the goals of the project?
With this project, we will build the first open reference dataset of label-free hyperspectral signatures from defined epithelial tissue states in Drosophila.
We will establish a controlled ex vivo imaging workflow and collect baseline data from healthy epithelial tissue, then generate wounded and apoptotic states under matched conditions and image them in the same way.
After each hyperspectral acquisition, we will use fluorescent markers to independently validate cell boundaries and dying cells so every spectral profile is anchored in a known biological state. We will then process the data, extract and organise the spectral signatures, and assemble an openly shared dataset with clear metadata and documentation.
Our goal is to create a reliable first resource that others can use to compare results, calibrate analyses, and build future tools within one year.
Budget
This budget covers the minimum realistic costs needed to generate a biologically validated reference dataset of label-free hyperspectral signatures from defined epithelial tissue states. It supports hyperspectral imaging access, ex vivo Drosophila tissue preparation and culture, fluorescent validation of cell boundaries and apoptotic cells, fly husbandry and imaging supplies, and essential data processing, storage, and platform fees. The target is intentionally kept modest while remaining sufficient to deliver a rigorous, openly shareable, field-building proof-of-concept resource that other researchers can use to compare results, calibrate analyses, and build future tools.
Endorsed by
Project Timeline
From September to November, we will establish the ex vivo workflow and collect baseline hyperspectral data from healthy tissue. From December to February, we will generate wounded and apoptotic states and image them under controlled conditions. From March to April, we will validate the data with fluorescent markers. From May to June, we will process results and assemble the reference dataset. In July 2027, we will release the dataset, documentation, and a plain-language summary for supporters.
Aug 17, 2026
Project Launched
Sep 01, 2026
Establish ex vivo imaging workflow for reproducible label-free hyperspectral acquisition
Nov 01, 2026
Complete baseline hyperspectral dataset from healthy epithelial tissue
Jan 01, 2027
Complete hyperspectral dataset from wounded epithelial tissue
Feb 01, 2027
Complete hyperspectral dataset from apoptotic epithelial tissue
Meet the Team
Affiliates
This project is led by Marisa Merino, a developmental biologist and imaging-focused researcher at the University of Liverpool. Her work centres on how tissues preserve order across growth, repair, and cell death, and this project builds directly on that experience to create an open, biologically validated resource for hyperspectral biology.
Marisa Merino
I am a Lecturer and Research Group Leader at the University of Liverpool. My research asks how tissues preserve order as they grow, repair damage, and eliminate unfit cells, and how these control systems become hijacked in disease. I work mainly with Drosophila, a powerful model for understanding how living tissues organise growth, cell death, and signalling in space.
I am fascinated by how living tissues maintain order while constantly changing, and this drives my interest in imaging-based approaches that let us see biology more directly and quantitatively. In this project, that comes together with a simple but important question: can healthy, wounded, and dying epithelial tissue be distinguished by label-free hyperspectral imaging?
I have a background in developmental biology, cell competition, imaging, and quantitative tissue analysis, and I have published work on cell fitness, cell death, and morphogen signalling. My goal here is to build a small but useful open reference dataset that others can use to compare results, calibrate new analyses, and develop future tools. I care about making resources that are both biologically rigorous and genuinely useful to other researchers.
Lab Notes
Nothing posted yet.
Additional Information
All data, metadata, and analysis documentation will be organised for open release as a reusable reference for future hyperspectral biology studies.
Project Backers
- 1Backers
- 110%Funded
- $6,050Total Donations
- $6,050.00Average Donation


