Credit: Nucleic Acids Research (2025). DOI: 10.1093/nar/gkaf1128

Researchers from Turku Bioscience Center at the University of Turku, Finland, have developed a new computational method to interpret complex single-cell data. The method helps researchers identify and group cell types across samples.

The human body contains about 37 trillion cells. Some are more alike than others, yet never exactly the same. Modern single-cell technologies allow characterizing this cellular heterogeneity, measuring dozens to thousands of molecules, such as genes or proteins, across thousands of individual cells simultaneously and providing insights into health and diseases.

A small amount of blood contains billions of red blood cells and millions of immune cells. Each type of cell has its own molecular “fingerprint,” which researchers can identify by combining single-cell technologies with computational methods.

When studying several different samples, scientists must first match the same cell types across the samples. This is a demanding step known as data integration. However, current integration methods often struggle when cell types vary between samples or appear in very different amounts. In such cases of imbalanced data, methods can mistakenly combine distinct cell types.

To solve this, researchers from the University of Turku have now developed a new machine learning-based algorithm that effectively integrates even imbalanced data across samples. The method, called Coralysis, has been developed at Turku Bioscience Center in Professor Laura Elo’s Computational Biomedicine research group, which is also affiliated with the InFLAMES Research Flagship.

“Single-cell technologies let us study the incredible diversity of cells, but comparing them across samples is tricky. This motivated us to develop a method to uncover these hidden patterns reliably,” says Associate Professor Sini Junttila, one of the supervisors of the study now published in Nucleic Acids Research.

Effective open-source tool

“We were inspired by the process of assembling a puzzle, where one begins by grouping pieces based on low- to high-level features, such as color and shading, before looking at shape and patterns. Similarly, our algorithm progressively integrates cellular identities through multiple rounds of divisive clustering,” explains Doctoral Researcher António Sousa, the lead developer of Coralysis.

Coralysis has been implemented as an open-source software. At its core, it relies on machine learning, enabling it to build models that can be used to predict cellular identities in new datasets and even estimate how confident the predictions are. This helps researchers avoid the cumbersome and often unreliable task of manually identifying cell types. Another unique feature of Coralysis is its ability to detect changing cellular states that might otherwise be missed.

“Coralysis provides the scientific community with a new way to study cellular diversity and gain a deeper understanding of complex single-cell data. By making it openly available, we hope to support collaboration and accelerate discoveries across the global research community,” says Professor Laura Elo, the principal investigator of the project.

More information: António G G Sousa et al, Coralysis enables sensitive identification of imbalanced cell types and states in single-cell data via multi-level integration, Nucleic Acids Research (2025). DOI: 10.1093/nar/gkaf1128

Citation: New computational tool helps scientists interpret complex single-cell data (2025, November 17) retrieved 17 November 2025 from https://phys.org/news/2025-11-tool-scientists-complex-cell.html

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