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. 2015 Feb 19;31(13):2141–2150. doi: 10.1093/bioinformatics/btv101

Table 1.

Performance comparison on simulated virus population:

ViVan LoFreq VPhaser2 SAMTools pileup
True positives 231 219 196 244
False positives 4 1 2 1399
True negatives 31918 31921 31920 30523
False negatives 13 25 48 0
sensitivity 0.947 0.898 0.803 1.000
specificity 1.000 1.000 1.000 0.956
PPV 0.983 0.995 0.990 0.149
NPV 0.999 0.998 0.995 1.000
F1-Score 0.965 0.944 0.887 0.259

Simulated DENV population using six sequenced clinical samples sub-sampled at various rates was used to demonstrate ViVan’s performance in the context of real sequencing data

Because the coverage in this data set was low (100×) ViVan’s PPV was the lowest. However, ViVan demonstrated the highest sensitivity out of the three methods, identifying all but one of the variants found in the other. This dataset also highlights the need for sequencing-error aware methods in order to reduce false positive calls such as the ones produced by naïve pileup.