Table 1 |
|
|
Probability of monophyletic origin for L90M sequences |
|
|
Patient |
p(monophyly) |
|
|
|
|
Multiple origins L90M |
|
|
|
|
|
608 |
0.05 |
|
6501 |
0.00 |
|
1125 |
0.00 |
|
1174 |
0.00 |
|
1317 |
0.00 |
|
|
|
|
Single origin L90M |
|
|
|
|
|
1124 |
0.99 |
|
4334 |
1.00 |
|
|
|
|
Inconclusive |
|
|
|
|
|
597 |
0.34 |
|
7071 |
0.29 |
|
1134 |
0.23 |
|
1329 |
0.14 |
|
1391 |
0.87 |
|
1527 |
0.30 |
|
1834 |
0.58 |
|
2091 |
0.18 |
|
|
|
|
The probability that sequences containing the L90M mutation within each patient were derived from a single (p≥0.95) or multiple (p≤0.05) mutation events, given as the proportion of 9000 trees drawn from the posterior distribution of the Bayesian MCMC analysis in which the sequences with the L90M mutations formed a monophyletic clade. |
|
|
Kapoor et al. Retrovirology 2008 5:7 doi:10.1186/1742-4690-5-7 |
|
