Research Article

The Number of Candidate Variants in Exome Sequencing for Mendelian Disease under No Genetic Heterogeneity

Table 4

The expected number of SNVs after filtering in dominant disease using full-sibs.






/ : 100% / : 90% / : 80% / : 100% ( )
0% ( )
/ : 100% ( )
0% ( )
/ : ≥80% ( )
0% ( )
/ : ≥80% ( )
0% ( )
/ : ≥80% ( )
≤20% ( )

119999.50
215832.94 4166.56 4166.56
313541.33 2291.61
412239.28 989.56 1302.05
511471.07 15312.12 768.21
1010263.05 11227.51 13064.81 14.05 96.45 512.68
1110193.97 69.08 948.55
1310106.96 36.82 127.64
2010013.86 10408.02 11922.23 0.01 4.71 40.85
2110010.33 3.53 500.32
2310005.70 1.98 38.66
509999.75 10031.07 11165.22 0.00 0.06
519999.75 291.41
539999.75 18.23
1009999.75 10000.36 10661.20