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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