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Abstract Long-read amplicon sequencing can profile longer sequences compared to short reads, but recovering amplicon sequence variants (ASVs) is a challenge for long, noisy reads. We present savont, an algorithm for recovering ASVs from modern long-read amplicons with mean accuracy ≥ 98%, including Oxford Nanopore Technologies (ONT) R10.4 and PacBio HiFi reads. Savont requires 5 to 16 times lower sequencing depth for full-length 16S rRNA ONT reads than previous methods and generates up to 95 times more ASVs for complex environments. Savont makes ASV-based analysis from shallow and noisy long-read amplicon sequencing feasible.
Shaw et al. (Fri,) studied this question.