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If it had not found any, it would have created with probability P tree a new tree with one branch from a random sequence of actions.
If there is no tree matching the event ((delta _{j}~=~varnothing )), with a certain probability P tree, the morwi forms a sequence from random events in (E_{in}^{M}).
Next, we combine the three probability vectors as follows: (1) C combined = 0. 4 × P tree + 0. 5 × P flat + 0. 1 × P knn, where the three combination weights are determined using held-out development data.
For any singleton s from P, tree S s) contains the single leaf (the root) s and the root tube; its cost is zero if there are no paralogous trees for s and is the cost of one duplication multiplied by ∑ j Par G j, s) otherwise (refer to Lemma 5).
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Bootstrap resampling of the NJ and P trees (1,000 and 100 replicates, respectively) was performed to provide statistical confidence to the topologies inferred.
The parental (P) trees AC3065 and Y3088 were plus-trees originating from north Sweden (latitudes 65°08′N and 64°09′N, respectively) selected for the Swedish Scots pine breeding program based on their vitality, rapid growth, small branch diameters, and wide branch angles.
Every p-tree is 2-clique-colourable by Theorem 8.
If G is a separable p-tree then it is 2-clique-colourable by Theorem 5.
If n=q then G is a p-tree, which is 2-clique-colourable by Theorem 8.
A p-forest G is either a serial graph or a decomposable neighbourhood graph or a p-tree.
From Theorem 7, it follows that the only homogeneous sets of a p-tree are the cographs eventually replacing the p-end-vertices of G.
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CEO of Professional Science Editing for Scientists @ prosciediting.com