Alternatively, inferences about the topology of the network can be made by introducing pulse changes in concentration of a chemical species in the network, and observing the network's response, concluding causal chemical connectivities [ 6].
Alternatively, their inference may reflect bioinformatic artifacts, such as imperfect gene annotation of the D-genome, or alternative stops that independently evolved in the A-genomes.
Alternatively, Bayesian inference of character evolution methods such as the character diffusion model (Ronquist 2004; Lemey et al. 2009) are currently being developed for the study of CST in RNA viruses such as rabies (Streicker et al. 2010; Faria et al. 2013) and account for tree uncertainty and more complex scenarios.
Alternatively, without bootstrapping, the frequencies of the haplotypes in the phased genotypes of all computed alternative inferences can be used similar to bootstrapping counts.
Alternatively, making inferences on the effective connectivity between reading areas may circumvent this spatial overlap problem and be more suitable for revealing neuro-functional links underlying the DRC model while teasing apart different theoretical viewpoints [13].
Alternatively, evolutionary inferences based on the RNAP III transcription machinery may be different from those of the genes that generally have been used to examine phylogenetic relationships in animals, fungi, and plants.
Alternatively, a conditional inference tree with recursive partitioning was constructed.
Alternatively, Wald type inference can be drawn with its MLE and variance.
Alternatively, the experimental haplotype inference may have missed rare but real haplotypes owing to underrepresentation of the sequence in the cloned amplicons.
Alternatively, work backwards through inference.
