From: In the light of deep coalescence: revisiting trees within networks
Gene Tree T i | P(T i |ψ,y,γ) |
---|---|
T 1=(((b,c),a),d) | \(\gamma -(\gamma -\frac {\gamma ^{2}}{3})e^{-y}\) |
T 2=(((b,c),d),a) | \((1-\gamma)-(-\frac {\gamma ^{2}}{3}-\frac {\gamma }{3}+\frac {2}{3})e^{-y}\) |
T 3=((a,b),(c,d)) | γ(1−γ)e −y |
T 4=((a,c),(b,d)) | γ(1−γ)e −y |
T 5=(((a,b),c),d) | \(\frac {\gamma ^{2}}{3}e^{-y}\) |
T 6=(((a,c),b),d) | \(\frac {\gamma ^{2}}{3}e^{-y}\) |
T 7=(a,(b,(c,d))) | \(\frac {(1-\gamma)^{2}}{3}e^{-y}\) |
T 8=(((b,d),c),a) | \(\frac {(1-\gamma)^{2}}{3}e^{-y}\) |
T 9=((a,d),(b,c)) | 0 |
T 10=(((a,b),d),c) | 0 |
T 11=(b,(a,(c,d))) | 0 |
T 12=(((a,d),b),c) | 0 |
T 13=(((b,d),a),c) | 0 |
T 14=(((a,c),d),b) | 0 |
T 15=(((a,d),c),b) | 0 |