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Article

miniSNV: accurate and fast single nucleotide variant calling from nanopore sequencing data.

Briefings in bioinformatics - 23 Sept 2024

Cui Miao, Liu Yadong, Yu Xian, Guo Hongzhe, Jiang Tao, Wang Yadong, Liu Bo

Abstract excerpt

Nanopore sequence technology has demonstrated a longer read length and enabled to potentially address the limitations of short-read sequencing including long-range haplotype phasing and accurate variant calling. However, there is still room for improvement in terms of the performance of single nucleotide variant (SNV) identification and computing resource usage for the state-of-the-art approaches. In this work,...

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PMID: 39331016
DOI: 10.1093/bib/bbae473
PMCID: PMC11428505

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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