A novel visualization tool to assess diversity in NGS data. Similar to the Los Alamos Highlighter tool, highlineR highlights mismatches, transition and transversion mutations, and synonymous and non-synonymous mutations in aligned protein or nucleotide sequences. This tool also visualizes the relative frequency of sequence variants and is particularly useful for visualizing sequence diversity, potential recombination and super-infection.
Package details |
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Maintainer | |
License | GPL-3 |
Version | 0.1 |
Package repository | View on GitHub |
Installation |
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