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All groups were supported by bootstrap values of 80% 100% (Technical Appendix) and were found by using alternative phylogenetic algorithms (maximum parsimony and maximum likelihood) (data not shown).
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This paper investigates the joint maximum likelihood (ML) data detection and channel estimation problem for Alamouti space-time block-coded (STBC) orthogonal frequency-division multiplexing (OFDM) wireless systems.
A similar branching pattern was obtained with the maximum likelihood method (data not shown).
Similar tree topologies were obtained by the maximum likelihood method (data not shown).
The GMYC method applied to the reduced sympatric dataset delimited three species at the maximum likelihood solution (data not shown).
This division of the dataset continued until we obtained reproducible topology of the human Rhodopsins in neighbor joining, maximum parsimony and maximum likelihood analyses (data not shown).
Distance optimality, neighbor-joining and parsimony based methods had lower support for most clades, but were compatible with the maximum likelihood phylogeny (data not shown).
The results of the Bayesian analysis of the path coefficients were very similar to the maximum likelihood estimates (data not shown) and will not be presented.
We found significant associations between U-Cd, on the one hand, and NAG, protein HC (both positive associations), and estimated GFR (negative association), on the other, based on the maximum likelihood model (data not shown).
In addition, we chose the GY method to compute Ka as an estimator of evolutionary rates, since counting methods usually yield more out-of-range values than maximum likelihood methods (data not shown).
Inferred relationships between genes were largely similar using the two approaches, although the relationship of LP 7 and LP 8 was unresolved using the Maximum Likelihood approach (data not shown).
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