Nature Computational ScienceBioinformaticsPeer-reviewed journal article
Symphonizing pileup and full-alignment for deep learning-based long-read variant calling
Zhenxian ZhengiD, Shumin LiiD, Junhao SuiD, Amy Wing-Sze LeungiD, Tak‐Wah LamiD, Ruibang LuoiD
Abstract
Deep learning-based variant callers are becoming the standard and have achieved superior SNP calling performance using long reads. In this paper, we present Clair3, which leveraged the best of two major method categories: pile-up calling handles most variant candidates with speed, and full-alignment tackles complicated candidates to maximize precision and recall. Clair3 ran faster than any of the other state-of-the-art variant callers and performed the best, especially at lower coverage.
- assay: whole-genome sequencing
- assay: long-read sequencing
- research focus: variant calling
- research focus: variant effect prediction
- approach: deep learning
- Citations
- 411
- FWCI
- 23.25
- Field percentile
- top 1%
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