Correction: Enhancing SNV identification in whole-genome sequencing data through the incorporation of known genetic variants into the minimap2 index.
作者信息
Guguchkin Egor, Kasianov Artem, Belenikin Maksim, Zobkova Gaukhar, Kosova Ekaterina, Makeev Vsevolod, Karpulevich Evgeny
机构信息
Ivannikov Institute for System Programming, Moscow, Russia.
Institute for Information Transmission Problems, Moscow, Russia.
出版信息
BMC Bioinformatics. 2024 Aug 19;25(1):268. doi: 10.1186/s12859-024-05892-6.
Abstract
摘要
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Correction: Enhancing SNV identification in whole-genome sequencing data through the incorporation of known genetic variants into the minimap2 index.更正：通过将已知遗传变异纳入minimap2索引来增强全基因组测序数据中的单核苷酸变异识别。
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本文引用的文献
1
Enhancing SNV identification in whole-genome sequencing data through the incorporation of known genetic variants into the minimap2 index.通过将已知遗传变异纳入 minimap2 索引来提高全基因组测序数据中 SNV 的识别能力。
BMC Bioinformatics. 2024 Jul 13;25(1):238. doi: 10.1186/s12859-024-05862-y.
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