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. 2017 May 16;206(3):1285–1295. doi: 10.1534/genetics.116.197491

Table 1 Effect of the selected threshold for minimal twin group size ts0 on the skeletal map length under low and moderate rates of genotyping errors and 20% of missing data points.

Map Initial After cleaning After saturation δ
pe Nm ts0 Nsk L Nsk L Nsk L
0.01 104 4 349 384.2 81 172.1 99 171.8 1.8
6 128 221.0 65 173.8 77 174.9 2.3
8 108 237.0 47 175.5 65 174.2 2.7
0.02 3 237 397.8 58 207.3 71 187.9 2.7
4 102 213.8 38 128.8 47 126.6 2.8
0.01 2 × 104 6 398 472.1 97 216.1 111 217.1 2.0
8 256 357.9 91 219.9 104 217.4 2.1
10 178 307.3 71 205.8 83 201.7 2.5
0.02 4 305 406.4 85 208.0 103 200.9 2.0
5 175 333.6 57 207.6 73 194.3 2.7
6 110 200.6 42 135.1 56 132.5 2.4
0.01 4 × 104 10 377 461.7 140 244.7 150 253.2 1.7
12 281 399.4 110 244.7 120 243.5 2.0
16 195 339.0 95 245.0 108 248.4 2.3
0.02 6 289 446.0 89 262.4 115 249.1 2.2
8 157 364.9 67 272.9 83 254.4 3.1
10 94 323.6 50 283.0 67 252.2 3.8

Simulated map length was L = 191.3, 214.6, and 273 cM for populations with Nm = 104, 2 × 104, and 4 × 104 markers, respectively; pe, level of genotyping errors per marker locus; ts, twin group size, ts0, threshold ts value: skeletal markers should obey the condition tsts0; Nsk, number of intervals in the map; Nm, number of markers per LG in the initial dataset; δ, map density (the ratio of the entire chromosome map length to the number of intervals).