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To the best of our knowledge, none of the previous methods have considered sensor noise model and estimated error and variance in order to adapt the reconstructed kernel for each local region of the image.
Finally, results and future work are discussed in Section 5. Due to limitations of the blind or the semi-blind approach for challenging estimation problems like audio source separation, recent methods have considered the usage of side information to improve the resulting quality for practical applications[9, 10].
However, none of these methods have considered both aspects of functional coherence, nor have they explicitly considered the relationships among GO terms co-annotating genes, which provide additional biological information.
To our knowledge, no studies of GS methods have considered epistatic genetic architectures, although Gianola et al. (2006) predicted nonparametric methods would be better-suited for epistatic genetic architectures.
Other methods have considered treating emergence and most-recent duplication events independently [ 6, 50], but this complicates the ability to study evolutionary distributions of large sets of genes and has not yet been applied to newly sequenced genomes.
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Earlier studies on the topology optimization method have considered EFCs or dispersion curves; however, there is no topology optimization that considers the EFC and FP simultaneously.
Not being interested in a routine method, having considered it but not being organized yet and doing an activity that provided a reminder on treatment increased the noncompliance compared always taking or applying the medication always at the same hour.
In addition, our method has considered the effects of sampling and data processing so that the user can justify whether a conclusion is sensitive to the high throughput-dependent noise.
Previous studies have revealed that specific backbone conformations are likely to be a part of ligand-binding site and that the magnitude of dihedral angles may undergo slight changes after ligand binding [ 13, 15, 19]; however, no method has considered the conformation of amino acids in ligand-binding site prediction.
To compare the performance of different fusion methods, we have considered the Friedman test [39].
In the proposed method, we have considered parameteric uncertainties based on assumption 2 for two chaotic systems with some candidate of parameter perturbations.
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