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A Composite interaction Score: Prioritizing cell-cell interactions from single-cell RNA-seq with application to

Olha Kholod1, Hien M Bui1, H Robert Frost2

  • 1Thayer School of Engineering, Dartmouth College, Hanover NH 03755, Germany.

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|March 24, 2026
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Summary

We developed a new method, the Composite Interaction Score (CIS), to better rank cell-cell interactions (CCIs) from single-cell RNA sequencing data. CIS prioritizes reproducible and biologically relevant CCIs, outperforming older methods and revealing key interactions in epithelial barrier tissues.

Keywords:
Cell–cell interactionsEpithelial barriersPre-menopausalscRNA-seq

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Area of Science:

  • Computational biology
  • Genomics
  • Immunology

Background:

  • Cell-cell interactions (CCIs) are crucial for tissue health and immune responses.
  • Current computational tools for inferring CCIs from single-cell RNA sequencing (scRNA-seq) data lack a standardized framework for result prioritization.
  • Existing consensus strategies often fail to identify the most biologically significant CCIs.

Purpose of the Study:

  • To develop a novel ranking strategy for CCIs that emphasizes reproducibility and biological relevance.
  • To apply this strategy to investigate CCIs within epithelial barrier tissues.

Main Methods:

  • Introduction of the Composite Interaction Score (CIS), a consensus metric integrating predictions from six CCI inference tools using the LIgand-receptor ANAlysis (LIANA) package.
  • Implementation of ranked-biased precision to weight tool agreement, prioritizing top-ranked concordant interactions.
  • Benchmarking CIS against a naive average-rank method using perturbed datasets to assess precision and recall.

Main Results:

  • CIS demonstrated superior performance over the average-rank baseline, achieving higher sensitivity and specificity in identifying true CCIs.
  • Application of CIS to scRNA-seq data from the intestine, skin, and uterus revealed both conserved and tissue-specific CCIs.
  • Identified key conserved interactions (e.g., MIF-CD74, APP-CD74) and highlighted tissue-specific crosstalk, such as GUCA2A/GUCA2B-GUCY2C in the intestine and SPP1-PTGER4 in the uterus.

Conclusions:

  • CIS offers a generalizable and effective framework for prioritizing CCIs from scRNA-seq data, surpassing naive consensus methods.
  • The study establishes a valuable resource for distinguishing conserved and tissue-specific communication networks in epithelial barriers.
  • Findings provide novel insights into barrier tissue function and pre-menopausal biology.