Figure 2From: Towards accurate detection and genotyping of expressed variants from whole transcriptome sequencing dataAccuracy comparison for four different SNV detection methods on the NA12878 hard merged alignments. The tradeoff between sensitivity and specificity is controlled in the Bayesian methods (SNVQ, SOAPsnp, and Maq) by varying the minimum probability of having a genotype different than the reference, while in PMA it is controlled by varying the maximum p-value required to reject the null hypothesis of absence of variants.Back to article page