Abstract 6860: Ensemble somatic variant calling and transcript reconstruction for high-fidelity neoantigen discovery in mRNA cancer vaccine design.

Abstract Personalized neoantigen vaccines require accurate identification of tumor-specific epitopes with clinical-grade confidence. However, pipelines that rely on single-caller somatic variant detection and reference-based transcript reconstruction often inflate false-positive neoantigens and mishandle complex mutations such as frameshifts and stop-codon disruptions, limiting the fidelity of candidates for mRNA cancer vaccines. We developed a GPU-accelerated workflow integrating whole-exome sequencing (WES) and RNA-seq, implemented on NVIDIA Parabricks to achieve more than a tenfold reduction in preprocessing time compared with conventional CPU-based pipelines. Somatic variants are identified using an ensemble consensus (≥2 of DeepSomatic, Strelka2 and VarScan), reducing inter-caller discordance while preserving biologically plausible events; germline variants are called with GATK HaplotypeCaller. To support neoepitope generation, we implemented a transcript reconstruction module that integrates all germline and somatic variants into patient-specific, strand-aware open reading frames, applies context-dependent peptide trimming (for example, ±20 amino acids for SNVs and dynamic windows for indels), and validates candidate coding changes against sequencing evidence, resolving multi-isoform usage and early terminations. Benchmarked on clinical solid tumor samples, the ensemble strategy improved reproducibility across technical replicates and showed high concordance with orthogonal variant validation. The reconstruction module robustly recovered mutant transcripts in diverse genomic contexts and enabled precise neoepitope extraction and HLA-binding prediction. Integrated with HLA genotyping and MHC binding models, this reproducible pipeline mitigates upstream sources of epitope inflation and provides a scalable bioinformatics framework for high-fidelity neoantigen discovery in personalized mRNA cancer vaccine design. Citation Format: Po-Yuan Chen, Mi-Hua Tao, Tai-Ming Ko. Ensemble somatic variant calling and transcript reconstruction for high-fidelity neoantigen discovery in mRNA cancer vaccine design [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2026; Part 1 (Regular Abstracts); 2026 Apr 17-22; San Diego, CA. Philadelphia (PA): AACR; Cancer Res 2026;86(7 Suppl):Abstract nr 6860.

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Journal
Cancer Research
Published
2026-04-03
DOI
https://doi.org/10.1158/1538-7445.am2026-6860
Primary Topic
vaccines and immunoinformatics approaches
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article
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article

Abstract 6860: Ensemble somatic variant calling and transcript reconstruction for high-fidelity neoantigen discovery in mRNA cancer vaccine design.

Po-Yuan Chen, Mi‐Hua Tao, Tai-Ming Ko
Cancer Research
vaccines and immunoinformatics approaches
article

Abstract 6860: Ensemble somatic variant calling and transcript reconstruction for high-fidelity neoantigen discovery in mRNA cancer vaccine design.

Po-Yuan Chen, Mi‐Hua Tao, Tai-Ming Ko
article en

Abstract

Abstract Personalized neoantigen vaccines require accurate identification of tumor-specific epitopes with clinical-grade confidence. However, pipelines that rely on single-caller somatic variant detection and reference-based transcript reconstruction often inflate false-positive neoantigens and mishandle complex mutations such as frameshifts and stop-codon disruptions, limiting the fidelity of candidates for mRNA cancer vaccines. We developed a GPU-accelerated workflow integrating whole-exome sequencing (WES) and RNA-seq, implemented on NVIDIA Parabricks to achieve more than a tenfold reduction in preprocessing time compared with conventional CPU-based pipelines. Somatic variants are identified using an ensemble consensus (≥2 of DeepSomatic, Strelka2 and VarScan), reducing inter-caller discordance while preserving biologically plausible events; germline variants are called with GATK HaplotypeCaller. To support neoepitope generation, we implemented a transcript reconstruction module that integrates all germline and somatic variants into patient-specific, strand-aware open reading frames, applies context-dependent peptide trimming (for example, ±20 amino acids for SNVs and dynamic windows for indels), and validates candidate coding changes against sequencing evidence, resolving multi-isoform usage and early terminations. Benchmarked on clinical solid tumor samples, the ensemble strategy improved reproducibility across technical replicates and showed high concordance with orthogonal variant validation. The reconstruction module robustly recovered mutant transcripts in diverse genomic contexts and enabled precise neoepitope extraction and HLA-binding prediction. Integrated with HLA genotyping and MHC binding models, this reproducible pipeline mitigates upstream sources of epitope inflation and provides a scalable bioinformatics framework for high-fidelity neoantigen discovery in personalized mRNA cancer vaccine design. Citation Format: Po-Yuan Chen, Mi-Hua Tao, Tai-Ming Ko. Ensemble somatic variant calling and transcript reconstruction for high-fidelity neoantigen discovery in mRNA cancer vaccine design [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2026; Part 1 (Regular Abstracts); 2026 Apr 17-22; San Diego, CA. Philadelphia (PA): AACR; Cancer Res 2026;86(7 Suppl):Abstract nr 6860.

Cancer ResearchVol. 86(7_Supplement)
National Yang Ming Chiao Tung University (TW), Academia Sinica (TW)
Quality Education
Openalex Percentile: Top 29%
vaccines and immunoinformatics approaches
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