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Factored HMMs offer computational benefits when computing the likelihood of data.
We model the recombination probabilities as P(S i j | S i −1 j ≠ S i j ) = 1 − e− l, where l is the genetic distance, in Morgans, between location i and i − 1. Factorial HMMs offer computational benefits when computing the likelihood of data.
It is the purpose of this paper to illustrate these concepts by presenting eHabitat, a basic Web Processing Service (WPS) for computing the likelihood of finding ecosystems with equal properties to those specified by a user.
This is followed by computing the likelihood of dominant supports within a cluster using (9) and E [ α S | r ] using (8).
Parameters for mass error and peak intensity can be chosen individually for each dataset, and are required for computing the likelihood of the data.
However, SNAP does consider the composition of each sequence element in computing the likelihood of particular gene models, and sequence changes within these elements may affect the likelihood of alternative gene models or states (e.g. no gene) enough to alter SNAP's predictions.
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The ML sequence of actions and their likelihoods over a number of time steps is used to find the most likely behaviour by computing the likelihoods of each of the predefined normal behaviour HMMs explaining the current action sequence.
Computing the likelihoods of patterns of genetic events for a given model is done using the functions likelihoods and distribution.
Confidence intervals around marker positions were estimated by computing the likelihoods of each marker in all possible positions, while preserving the final order of remaining markers in the linkage group.
Therefore, we discretize the Cartesian space into voxels and compute the likelihood of the voxel being on a hidden surface.
In robot localization, these mappings are used to compute the likelihood of locations conditioned to new sensor measurements.
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