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CABE-RY: A PAM-flexible dual-mutation base editor for reliable modeling of multi-nucleotide variants



Genomic surveillance of Nevada patients revealed prevalence of unique SARS-CoV-2 variants bearing mutations in the RdRp gene



Vcflib and tools for processing the VCF variant call format



Watch Out for a Second SNP: Focus on Multi-Nucleotide Variants in Coding Regions and Rescued Stop-Gained


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Multi Nucleotide Variants
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