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    Correction: enhancing SNV identification in whole-genome sequencing data through the incorporation of known genetic variants into the minimap2 index

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    Authors
    Guguchkin, E.
    Kasianov, A.
    Belenikin, M.
    Zobkova, G.
    Kosova, E.
    Makeev, Vsevolod
    Karpulevich, E.
    Affiliation
    Cancer Research UK National Biomarker Centre, University of Manchester, Manchester, Manchester, M20 4BX, UK.
    Issue Date
    2024
    
    Metadata
    Show full item record
    Citation
    Guguchkin E, Kasianov A, Belenikin M, Zobkova G, Kosova E, Makeev V, et al. Correction: Enhancing SNV identification in whole-genome sequencing data through the incorporation of known genetic variants into the minimap2 index. BMC bioinformatics. 2024 Aug 19;25(1):268. PubMed PMID: 39160494. Pubmed Central PMCID: PMC11334595. Epub 2024/08/20. eng.
    Journal
    BMC Bioinformatics
    URI
    http://hdl.handle.net/10541/627194
    DOI
    10.1186/s12859-024-05892-6
    PubMed ID
    39160494
    Additional Links
    https://dx.doi.org/10.1186/s12859-024-05892-6
    Type
    Other
    Language
    en
    ae974a485f413a2113503eed53cd6c53
    10.1186/s12859-024-05892-6
    Scopus Count
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    All Paterson Institute for Cancer Research

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