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A New Approach of Detecting ALK Fusion Oncogenes by RNA Sequencing Exon Coverage Analysis.
Cancers (Basel). 2024 Nov 16;16(22):3851. doi: 10.3390/cancers16223851.
Cancers (Basel). 2024.
PMID: 39594806
Free PMC article.
Correction: Enhancing SNV identification in whole-genome sequencing data through the incorporation of known genetic variants into the minimap2 index.
Guguchkin E, Kasianov A, Belenikin M, Zobkova G, Kosova E, Makeev V, Karpulevich E.
Guguchkin E, et al.
BMC Bioinformatics. 2024 Aug 19;25(1):268. doi: 10.1186/s12859-024-05892-6.
BMC Bioinformatics. 2024.
PMID: 39160494
Free PMC article.
No abstract available.
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Enhancing SNV identification in whole-genome sequencing data through the incorporation of known genetic variants into the minimap2 index.
Guguchkin E, Kasianov A, Belenikin M, Zobkova G, Kosova E, Makeev V, Karpulevich E.
Guguchkin E, et al.
BMC Bioinformatics. 2024 Jul 13;25(1):238. doi: 10.1186/s12859-024-05862-y.
BMC Bioinformatics. 2024.
PMID: 39003441
Free PMC article.
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