计算机科学
共识序列
计算生物学
标识符
DNA测序
变压器
马尔可夫链
序列(生物学)
编码器
算法
生物
遗传学
基因
基序列
物理
电压
机器学习
操作系统
程序设计语言
量子力学
作者
Gunjan Baid,Daniel E. Cook,Kishwar Shafin,Taedong Yun,Felipe Llinares-López,Quentin Berthet,Anastasiya Belyaeva,Armin Töpfer,Aaron M. Wenger,William J. Rowell,Howard H. Yang,Alexey Kolesnikov,Waleed Ammar,Jean-Philippe Vert,Ashish Vaswani,Cory Y. McLean,Maria Nattestad,Pi-Chuan Chang,Andrew Carroll
标识
DOI:10.1038/s41587-022-01435-7
摘要
Circular consensus sequencing with Pacific Biosciences (PacBio) technology generates long (10–25 kilobases), accurate ‘HiFi’ reads by combining serial observations of a DNA molecule into a consensus sequence. The standard approach to consensus generation, pbccs, uses a hidden Markov model. We introduce DeepConsensus, which uses an alignment-based loss to train a gap-aware transformer–encoder for sequence correction. Compared to pbccs, DeepConsensus reduces read errors by 42%. This increases the yield of PacBio HiFi reads at Q20 by 9%, at Q30 by 27% and at Q40 by 90%. With two SMRT Cells of HG003, reads from DeepConsensus improve hifiasm assembly contiguity (NG50 4.9 megabases (Mb) to 17.2 Mb), increase gene completeness (94% to 97%), reduce the false gene duplication rate (1.1% to 0.5%), improve assembly base accuracy (Q43 to Q45) and reduce variant-calling errors by 24%. DeepConsensus models could be trained to the general problem of analyzing the alignment of other types of sequences, such as unique molecular identifiers or genome assemblies.
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