Correction: enhancing SNV identification in whole-genome sequencing data through the incorporation of known genetic variants into the minimap2 index
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Cancer Research UK National Biomarker Centre, University of Manchester, Manchester, Manchester, M20 4BX, UK.Issue Date
2024
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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 BioinformaticsDOI
10.1186/s12859-024-05892-6PubMed ID
39160494Additional Links
https://dx.doi.org/10.1186/s12859-024-05892-6Type
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enae974a485f413a2113503eed53cd6c53
10.1186/s12859-024-05892-6
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