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. 2010 Dec 15;85(5):2266–2275. doi: 10.1128/JVI.01396-10

FIG. 3.

FIG. 3.

Frequencies of mismatches (second data set) obtained by aligning the reads to the reference genome. (A) Inoculum; (B) FLF sample; (C) BRF sample. The second data set had a higher level of coverage than the first one, with a smaller fraction of sites with no mismatches. The average mismatch frequency is very similar to that of the first data set.