Heart rate variability (HRV) contains important information about the modulation of the cardiovascular system. Various methods of nonlinear dynamics (e.g., estimating Lyapunov exponents) and complexity measures (e.g., correlation dimension or entropies) have been applied to HRV analysis. Permutation entropy, which was proposed recently, has been widely used in many fields due to its conceptual and computational simplicity. It maps a time series onto a symbolic sequence of permutation ranks. The original permutation entropy assumes the time series under study has a continuous distribution, thus equal values are rare and can be ignored by ranking them according to their order of emergence, or broken by adding small random perturbations to ensure every symbol in a sequence is different. However, when the observed time series is digitized with lower resolution leading to a greater number of equal values, or the equalities represent certain characteristic sequential patterns of the system, it may not be rational to simply ignore or break them. In the present paper, a modified permutation entropy is proposed that, by mapping the equal value onto the same symbol (rank), allows for a more accurate characterization of system states. The application of the modified permutation entropy to the analysis of HRV is investigated using clinically collected data. Results show that modified permutation entropy can greatly improve the ability to distinguish the HRV signals under different physiological and pathological conditions. It can characterize the complexity of HRV more effectively than the original permutation entropy.

BackgroundBeta diversity, which involves the assessment of differences between communities, is an important problem in ecological studies. Many statistical methods have been developed to quantify beta diversity, and among them, UniFrac and weighted-UniFrac (W-UniFrac) are widely used. The W-UniFrac is a weighted sum of branch lengths in a phylogenetic tree of the sequences from the communities. However, W-UniFrac does not consider the variation of the weights under random sampling resulting in less power detecting the differences between communities.ResultsWe develop a new statistic termed variance adjusted weighted UniFrac (VAW-UniFrac) to compare two communities based on the phylogenetic relationships of the individuals. The VAW-UniFrac is used to test if the two communities are different. To test the power of VAW-UniFrac, we first ran a series of simulations which revealed that it always outperforms W-UniFrac, as well as UniFrac when the individuals are not uniformly distributed. Next, all three methods were applied to analyze three large 16S rRNA sequence collections, including human skin bacteria, mouse gut microbial communities, microbial communities from hypersaline soil and sediments, and a tropical forest census data. Both simulations and applications to real data show that VAW-UniFrac can satisfactorily measure differences between communities, considering not only the species composition but also abundance information.ConclusionsVAW-UniFrac can recover biological insights that cannot be revealed by other beta diversity measures, and it provides a novel alternative for comparing communities.

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