Article

SNooPy: a statistical framework for long-read metagenomic variant calling

2025-12-02

Abstract excerpt

Current long-read single-nucleotide variant callers were designed primarily for genomic data—particularly human genomes. While some have been used on metagenomic data, their underlying assumptions and training procedures fail to account for the inherent complexity of metagenomic samples. To date, no long-read variant caller has been purpose-built for metagenomic applications. To address this gap, we present SNooPy...

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Literature Corpus work: 900b87c2-a93a-547f-bf2e-b436043008f9
DOI: 10.64898/2025.12.01.691549

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