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Research: The body composition model is closely related to the physiological characteristics of the human body. At the same time there can be a large number of physiological characteristics, many of which may be redundant or irrelevant. In existing human physiological feature selection algorithms, it is difficult to overcome the impact that redundancy and irrelevancy may have on human body composition modeling. This suggests a role for selection algorithms, where human physiological characteristics are identified using a combination of filtering and improved clustering. To do this, a feature filtering method based on Hilbert-Schmidt dependency criteria is first of all used to eliminate irrelevant features. After this, it is possible to use improved Chameleon clustering to increase the combination of sub-clusters amongst the characteristics, thereby removing any redundant features to obtain a candidate feature set for human body composition modeling. Method We report here on the use of an algorithm to filter the characteristic parameters in INBODY770 (this paper used INBODY 770 as body composition analyzer.) measurement data, which has three commonly-used impedance bands (1 kHZ, 250 kHZ, 500 kHZ). This algorithm is able to filter out parameters that have a low correlation with body composition BFM. The algorithm is also able to draw upon improved clustering techniques to reduce the initial feature set from 29 parameters to 10 parameters for any parameters of the 250 kHZ band that remain after filtering. In addition, we also examined the impact of different sample sizes on feature selection. Result: The proposed algorithm is able to remove irrelevant and redundant features and the resulting correlation between the model and the body composition (BFM which is a whole body fat evaluation can better assess the body's overall fat and muscle composition.) is 0.978, thereby providing an improved model for prediction with a relative error of less than 0.12. [ABSTRACT FROM AUTHOR]

The sampling of scale-free networks in Molecular Biology is usually achieved by growing networks from a seed using recursive algorithms with elementary moves which include the addition and deletion of nodes and bonds. These algorithms include the Barabási-Albert algorithm. Later algorithms, such as the Duplication-Divergence algorithm, the Solé algorithm and the iSite algorithm, were inspired by biological processes underlying the evolution of protein networks, and the networks they produce differ essentially from networks grown by the Barabási-Albert algorithm. In this paper the mean field analysis of these algorithms is reconsidered, and extended to variant and modified implementations of the algorithms. The degree sequences of scale-free networks decay according to a powerlaw distribution, namely P(k) ∼ k− γ, where γ is a scaling exponent. We derive mean field expressions for γ, and test these by numerical simulations. Generally, good agreement is obtained. We also found that some algorithms do not produce scale-free networks (for example some variant Barabási-Albert and Solé networks). [ABSTRACT FROM AUTHOR]

Background: Non-coding RNAs perform a wide range of functions inside the living cells that are related to their structures. Several algorithms have been proposed to predict RNA secondary structure based on minimum free energy. Low prediction accuracy of these algorithms indicates that free energy alone is not sufficient to predict the functional secondary structure. Recently, the obtained information from the SHAPE experiment greatly improves the accuracy of RNA secondary structure prediction by adding this information to the thermodynamic free energy as pseudo-free energy. Method: In this paper, a new method is proposed to predict RNA secondary structure based on both free energy and SHAPE pseudo-free energy. For each RNA sequence, a population of secondary structures is constructed and their SHAPE data are simulated. Then, an evolutionary algorithm is used to improve each structure based on both free and pseudo-free energies. Finally, a structure with minimum summation of free and pseudo-free energies is considered as the predicted RNA secondary structure. Results and Conclusions: Computationally simulating the SHAPE data for a given RNA sequence requires its secondary structure. Here, we overcome this limitation by employing a population of secondary structures. This helps us to simulate the SHAPE data for any RNA sequence and consequently improves the accuracy of RNA secondary structure prediction as it is confirmed by our experiments. The source code and web server of our proposed method are freely available at . [ABSTRACT FROM AUTHOR]