ArticleCell genomics2026
scXpand: Pan-cancer detection of T cell clonal expansion from single-cell RNA sequencing without paired single-cell TCR sequencing.
Article in Cell genomics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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Abstract
Advances in single-cell sequencing have enabled detailed characterization of T cell clonal dynamics in cancer. However, analyses aiming to link the transcriptional landscape to T cell clonality remain limited by confounding factors unequally controlled in different studies. To address this challenge, we developed scXpand, a machine-learning framework for pan-cancer detection of T cell clonal expansion directly from single-cell RNA sequencing (scRNA-seq), without paired T cell receptor (TCR) sequencing. Trained and tested using our in-house-constructed human pan-cancer database of paired scRNA/TCR-seq profiles from 2.6 million T cells, scXpand demonstrates robust and accurate detection of clonal expansion across tissues and T cell subtypes. Applied to datasets lacking TCR sequencing, scXpand predictions correspond with known characteristics of the tumor microenvironment. Overall, scXpand provides a framework for detecting T cell clonal expansion across cancers directly from scRNA-seq, enabling broad use on datasets lacking scTCR-seq, while supporting scalable, memory-efficient processing, including pre-trained models with user-friendly documentation for flexible applications.
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