Symphonizing pileup and full-alignment for deep learning-based long-read variant calling

Nat Comput Sci. 2022 Dec;2(12):797-803. doi: 10.1038/s43588-022-00387-x. Epub 2022 Dec 19.

Abstract

Deep learning-based variant callers are becoming the standard and have achieved superior single nucleotide polymorphisms calling performance using long reads. Here we present Clair3, which leverages two major method categories: pileup calling handles most variant candidates with speed, and full-alignment tackles complicated candidates to maximize precision and recall. Clair3 runs faster than any of the other state-of-the-art variant callers and demonstrates improved performance, especially at lower coverage.

MeSH terms

  • Deep Learning*
  • High-Throughput Nucleotide Sequencing / methods
  • Polymorphism, Single Nucleotide / genetics