# CSpace: a concept embedding space for biomedical applications

**Authors:** Danilo Tomasoni, Luca Marchetti

PMC · DOI: 10.1093/bioinformatics/btaf376 · 2025-06-27

## TL;DR

CSpace is a biomedical concept embedding model that improves semantic search and concept-relatedness measurements with efficient performance.

## Contribution

CSpace introduces a concise biomedical embedding space that outperforms alternatives in semantic tasks and supports efficient concept-relatedness computation.

## Key findings

- CSpace achieves better out-of-vocabulary ratio and semantic textual similarity than existing models.
- It performs comparably to transformer-based models in sentence similarity tasks but with simpler architecture.
- CSpace integrates ontological identifiers for efficient disease, gene, and condition relatedness analysis.

## Abstract

The rise of transformer-based architectures has dramatically improved our ability to analyze natural language. However, the power and flexibility of these general-purpose models come at the cost of highly complex model architectures with billions of parameters that are not always needed.

In this work, we present CSpace: a concise word embedding of biomedical concepts that outperforms all alternatives in terms of out-of-vocabulary ratio and semantic textual similarity task, and has comparable performance with respect to transformer-based alternatives in the sentence similarity task. This ability can serve as the foundation for semantic search by enabling efficient retrieval of conceptually related terms. Additionally, CSpace incorporates ontological identifiers (MeSH, NCBI gene and taxonomy IDs), enabling computationally efficient disease, gene or condition relatedness measurement, potentially unlocking previously unknown disease-condition associations.

Full and compressed models are available on Zenodo at https://doi.org/10.5281/zenodo.14781672, while training code, examples, interactive visualizations and experiments are available at https://doi.org/10.5281/zenodo.15125706 and on the GitHub repository.

## Full-text entities

- **Genes:** MAPT (microtubule associated protein tau) [NCBI Gene 4137] {aka DDPAC, FTD1, FTDP-17, MAPTL, MSTD, MTBT1}
- **Diseases:** IPF (MESH:D065627), Fatigue Syndrome (MESH:D005221), Fibromyalgia (MESH:D005356), mycobacterial (MESH:C564468), Chronic Fatigue (MESH:D015673), Idiopathic Pulmonary Fibrosis (MESH:D054990), Tuberculosis (MESH:D014376), Long Covid (MESH:D000094024)
- **Chemicals:** CFS (-)
- **Species:** Homo sapiens (human, species) [taxon 9606], Mycobacterium tuberculosis (species) [taxon 1773]

## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12275461/full.md

---
Source: https://tomesphere.com/paper/PMC12275461