
AbstractIdentification of somatic mutations in tumor samples is commonly based on statistical methods in combination with heuristic filters. Here we develop VarNet, an end-to-end deep learning approach for identification of somatic variants from aligned tumor and matched normal DNA reads. VarNet is trained using image representations of 4.6 million high-confidence somatic variants annotated in 356 tumor whole genomes. We benchmark VarNet across a range of publicly available datasets, demonstrating performance often exceeding current state-of-the-art methods. Overall, our results demonstrate how a scalable deep learning approach could augment and potentially supplant human engineered features and heuristic filters in somatic variant calling.
Benchmarking, Deep Learning, Science, Neoplasms, Q, High-Throughput Nucleotide Sequencing, Humans, Article, Algorithms
Benchmarking, Deep Learning, Science, Neoplasms, Q, High-Throughput Nucleotide Sequencing, Humans, Article, Algorithms
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