Figure 6.

SNVQ genotyping accuracy on NA12878 hard merged alignments for varying number of lanes where each alternative allele must be seen. Results without filtering and with a threshold of at least two reads (regardless of their lanes of origin) are also included for comparison.

Duitama et al. BMC Genomics 2012 13(Suppl 2):S6   doi:10.1186/1471-2164-13-S2-S6