VDJdb in 2026: boosting T-cell receptor recognition evidence using paratope embeddings and AI-based structure prediction
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Updated: Sep 25, 2026

VDJ-Seq: Deep Sequencing Analysis of Rearranged Immunoglobulin Heavy Chain Gene to Reveal Clonal Evolution Patterns of B Cell Lymphoma
Published on: December 28, 2015
Daniil V Luppov1, Anna E Koneva1,2, Dmitry V Bagaev3
1Institute of Translational Medicine, Russian National Medical State University, 117513 Moscow, Russia.
Abstract:
We present a significant update to VDJdb, introducing substantial enhancements to both the data content and the technical infrastructure. The integration of steadily accumulating T-cell receptor (TCR):epitope recognition data, together with advances in high-throughput experimental techniques, has expanded the landscape for machine learning-based prediction of TCR specificity, covering foreign antigens, neoantigens, and autoimmunity-associated epitopes. However, these advances have introduced new challenges, most notably in data quality-large-scale assays have heightened concerns about measurement reliability and exacerbated existing issues such as HLA and epitope coverage biases. To address these issues, we have adopted state-of-the-art artificial intelligence approaches, including protein sequence embeddings and AI-driven structure prediction. The updated VDJdb resource now features TCR specificity records annotated with embedding-derived paratope features, advanced noise filtering capabilities, and predicted three-dimensional protein structures. These improvements enable more comprehensive interrogation of TCR-epitope recognition and provide novel lines of evidence to support the reliability of high-throughput assay records, which are frequently limited by insufficient independent validation. VDJdb can be accessed at https://vdjdb.com and https://github.com/antigenomics/vdjdb-db.
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