Single nucleotide variants, SNVs, between 18 asymptomatic carriage samples and most closely genetically related prior and subsequent symptomatic/asymptomatic sample.
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Participants are ordered by the number of SNVs to the most closely related sample. The participant numbering follows the same scheme used in Figure 2.*indicates acquisition following an initially negative sample.§indicates subsequently developed disease with the same strain,†indicates subsequently developed disease with a different strain.
创建时间：
2015-12-02
