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Accurate somatic variant detection using weakly supervised deep learning.
Krishnamachari, Kiran; Lu, Dylan; Swift-Scott, Alexander; Yeraliyev, Anuar; Lee, Kayla; Huang, Weitai; Leng, Sim Ngak; Skanderup, Anders Jacobsen.
Afiliação
  • Krishnamachari K; Department of Computational and Systems Biology, Agency for Science Technology and Research, Genome Institute of Singapore, Singapore, Singapore.
  • Lu D; School of Computing, National University of Singapore, Singapore, Singapore.
  • Swift-Scott A; Department of Computational and Systems Biology, Agency for Science Technology and Research, Genome Institute of Singapore, Singapore, Singapore.
  • Yeraliyev A; Department of Computational and Systems Biology, Agency for Science Technology and Research, Genome Institute of Singapore, Singapore, Singapore.
  • Lee K; Department of Computational and Systems Biology, Agency for Science Technology and Research, Genome Institute of Singapore, Singapore, Singapore.
  • Huang W; Department of Computational and Systems Biology, Agency for Science Technology and Research, Genome Institute of Singapore, Singapore, Singapore.
  • Leng SN; Department of Computational and Systems Biology, Agency for Science Technology and Research, Genome Institute of Singapore, Singapore, Singapore.
  • Skanderup AJ; Department of Computational and Systems Biology, Agency for Science Technology and Research, Genome Institute of Singapore, Singapore, Singapore.
Nat Commun ; 13(1): 4248, 2022 07 22.
Article em En | MEDLINE | ID: mdl-35869060
Identification 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.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Aprendizado Profundo / Neoplasias Tipo de estudo: Diagnostic_studies Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Aprendizado Profundo / Neoplasias Tipo de estudo: Diagnostic_studies Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article