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. 2020 Dec 9;11(12):1478. doi: 10.3390/genes11121478

Figure 8.

Figure 8

(A) A breakdown of the different calls (Table S2) for each sequencing coverage at a Q threshold of 13 for the 10,000 homozygous loci. (B) A breakdown of the different calls (Table S2) for each sequencing coverage at a Q threshold of 10 for the 10,000 homozygous loci. (C) A breakdown of the different calls (Table S2) for each sequencing coverage at a Q threshold of 7 for the 10,000 homozygous loci. (D) A breakdown of the different calls (Table S2) for each sequencing coverage at a Q threshold of 5 for the 10,000 homozygous loci.