Prostate-VarBench: A Benchmark with Interpretable TabNet Framework for Prostate Cancer Variant Classification

Fuente: arXiv
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Autores principales: Tavara, Abraham Francisco Arellano, Kumar, Umesh, Pradeepkumar, Jathurshan, Sun, Jimeng
Formato: Preprint
Publicado: 2025
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author Tavara, Abraham Francisco Arellano
Kumar, Umesh
Pradeepkumar, Jathurshan
Sun, Jimeng
author_facet Tavara, Abraham Francisco Arellano
Kumar, Umesh
Pradeepkumar, Jathurshan
Sun, Jimeng
contents Variants of Uncertain Significance (VUS) limit the clinical utility of prostate cancer genomics by delaying diagnosis and therapy when evidence for pathogenicity or benignity is incomplete. Progress is further limited by inconsistent annotations across sources and the absence of a prostate-specific benchmark for fair comparison. We introduce Prostate-VarBench, a curated pipeline for creating prostate-specific benchmarks that integrates COSMIC (somatic cancer mutations), ClinVar (expert-curated clinical variants), and TCGA-PRAD (prostate tumor genomics from The Cancer Genome Atlas) into a harmonized dataset of 193,278 variants supporting patient- or gene-aware splits to prevent data leakage. To ensure data integrity, we corrected a Variant Effect Predictor (VEP) issue that merged multiple transcript records, introducing ambiguity in clinical significance fields. We then standardized 56 interpretable features across eight clinically relevant tiers, including population frequency, variant type, and clinical context. AlphaMissense pathogenicity scores were incorporated to enhance missense variant classification and reduce VUS uncertainty. Building on this resource, we trained an interpretable TabNet model to classify variant pathogenicity, whose step-wise sparse masks provide per-case rationales consistent with molecular tumor board review practices. On the held-out test set, the model achieved 89.9% accuracy with balanced class metrics, and the VEP correction yields an 6.5% absolute reduction in VUS.
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id arxiv_https___arxiv_org_abs_2511_09576
institution arXiv
publishDate 2025
record_format arxiv
spellingShingle Prostate-VarBench: A Benchmark with Interpretable TabNet Framework for Prostate Cancer Variant Classification
Tavara, Abraham Francisco Arellano
Kumar, Umesh
Pradeepkumar, Jathurshan
Sun, Jimeng
Quantitative Methods
Artificial Intelligence
Machine Learning
Variants of Uncertain Significance (VUS) limit the clinical utility of prostate cancer genomics by delaying diagnosis and therapy when evidence for pathogenicity or benignity is incomplete. Progress is further limited by inconsistent annotations across sources and the absence of a prostate-specific benchmark for fair comparison. We introduce Prostate-VarBench, a curated pipeline for creating prostate-specific benchmarks that integrates COSMIC (somatic cancer mutations), ClinVar (expert-curated clinical variants), and TCGA-PRAD (prostate tumor genomics from The Cancer Genome Atlas) into a harmonized dataset of 193,278 variants supporting patient- or gene-aware splits to prevent data leakage. To ensure data integrity, we corrected a Variant Effect Predictor (VEP) issue that merged multiple transcript records, introducing ambiguity in clinical significance fields. We then standardized 56 interpretable features across eight clinically relevant tiers, including population frequency, variant type, and clinical context. AlphaMissense pathogenicity scores were incorporated to enhance missense variant classification and reduce VUS uncertainty. Building on this resource, we trained an interpretable TabNet model to classify variant pathogenicity, whose step-wise sparse masks provide per-case rationales consistent with molecular tumor board review practices. On the held-out test set, the model achieved 89.9% accuracy with balanced class metrics, and the VEP correction yields an 6.5% absolute reduction in VUS.
title Prostate-VarBench: A Benchmark with Interpretable TabNet Framework for Prostate Cancer Variant Classification
topic Quantitative Methods
Artificial Intelligence
Machine Learning
url https://arxiv.org/abs/2511.09576