Table 3 |
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| Pollen haplotypes and their respective frequencies for a male ABCD1234 with tetrasomic inheritance | |||||||||||
| Tetrasomic inheritance: β = 1 all Δ = 0 α = 0 | |||||||||||
| 0.17 | 0.17 | 0.17 | 0.17 | 0.17 | 0.17 | ||||||
| AB | AC | AD | BC | BD | CD | ||||||
| 0.17 | 12 | AB12 | AC12 | AD12 | BC12 | BD12 | CD12 | ||||
| 0.17 | 13 | AB13 | AC13 | AD13 | BC13 | BD13 | CD13 | ||||
| 0.17 | 14 | AB14 | AC14 | AD14 | BC14 | BD14 | CD14 | ||||
| 0.17 | 23 | AB23 | AC23 | AD23 | BC23 | BD23 | CD23 | ||||
| 0.17 | 24 | AB24 | AC24 | AD24 | BC24 | BD24 | CD24 | ||||
| 0.17 | 34 | AB34 | AC34 | AD34 | BC34 | BD34 | CD34 | ||||
| Tetrasomic Inheritance + Chromatid Segregation + Double Reduction β = 1 all Δ = 0 α = 0.14 | |||||||||||
| 0.14 | 0.14 | 0.14 | 0.14 | 0.14 | 0.14 | 0.04 | 0.04 | 0.04 | 0.04 | ||
| AB | AC | AD | BC | BD | CD | AA | BB | CC | DD | ||
| 0.17 | 12 | AB12 | AC12 | AD12 | BC12 | BD12 | CD12 | AA12 | BB12 | CC12 | DD12 |
| 0.17 | 13 | AB13 | AC13 | AD13 | BC13 | BD13 | CD13 | AA13 | BB13 | CC13 | DD13 |
| 0.17 | 14 | AB14 | AC14 | AD14 | BC14 | BD14 | CD14 | AA14 | BB14 | CC14 | DD14 |
| 0.17 | 23 | AB23 | AC23 | AD23 | BC23 | BD23 | CD23 | AA23 | BB23 | CC23 | DD24 |
| 0.17 | 24 | AB24 | AC24 | AD24 | BC24 | BD24 | CD24 | AA24 | BB24 | CC24 | DD24 |
| 0.17 | 34 | AB34 | AC34 | AD34 | BC34 | BD34 | CD34 | AA34 | BB34 | CC34 | DD34 |
| 0.04 | 11 | AB11 | AC11 | AD11 | BC11 | BD11 | CD11 | AA11 | BB11 | CC11 | DD11 |
| 0.04 | 22 | AB22 | AC22 | AD22 | BC22 | BD22 | CD22 | AA22 | BB22 | CC22 | DD22 |
| 0.04 | 33 | AB33 | AC33 | AD33 | BC33 | BD33 | CD33 | AA33 | BB33 | CC33 | DD33 |
| 0.04 | 44 | AB44 | AC44 | AD44 | BC44 | BD44 | CD44 | AA44 | BB44 | CC44 | DD44 |
Pure tetrasomic inheritance produces all 36 possible genotypes are shown in regular format. Haplotypes in bold are the ones formed by chromatid segregation and haplotypes in italic are formed by double reduction. The probabilities of each S or Z allele combination are given; the gamete frequency can be calculated as joined probability of the frequency at each locus.
Aguirre et al. BMC Bioinformatics 2012 13:125 doi:10.1186/1471-2105-13-125