Most real-world networks are too large to be measured or studied directly and there is substantial interest in estimating global network properties from smaller sub-samples. One of the most important global properties is the number of vertices/nodes in the network. Estimating the number of vertices in a large network is a major challenge in computer science, epidemiology, demography, and intelligence analysis. In this paper we consider a population random graph G = (V;E) from the stochastic block model (SBM) with K communities/blocks. A sample is obtained by randomly choosing a subset W and letting G(W) be the induced subgraph in G of the vertices in W. In addition to G(W), we observe the total degree of each sampled vertex and its block membership. Given this partial information, we propose an efficient PopULation Size Estimation algorithm, called PULSE, that accurately estimates the size of the whole population as well as the size of each community. To support our theoretical analysis, we perform an exhaustive set of experiments to study the effects of sample size, K, and SBM model parameters on the accuracy of the estimates. The experimental results also demonstrate that PULSE significantly outperforms a widely-used method called the network scale-up estimator in a wide variety of scenarios.
While they are very useful to diagnose typical cases, it is difficult for them to diagnose complicated cases. Therefore various approaches, such as deeper knowledge representation, case-based reasoning, are proposed in order to overcome this problem. However, they axe not sufficient to solve this problem completely. One reason that they are not so sutticient is that they are lacking one important track of diagnosis that medical experts do when they meet complicated cases. In this paper, we introduce combination of reasoning, planning and learning methods in order to solve this difficulty.
Predicated on the increasing abundance of electronic health records, we investigate the problem of inferring individualized treatment effects using observational data. Stemming from the potential outcomes model, we propose a novel multi-task learning framework in which factual and counterfactual outcomes are modeled as the outputs of a function in a vector-valued reproducing kernel Hilbert space (vvRKHS). We develop a nonparametric Bayesian method for learning the treatment effects using a multi-task Gaussian process (GP) with a linear coregionalization kernel as a prior over the vvRKHS. The Bayesian approach allows us to compute individualized measures of confidence in our estimates via pointwise credible intervals, which are crucial for realizing the full potential of precision medicine. The impact of selection bias is alleviated via a risk-based empirical Bayes method for adapting the multi-task GP prior, which jointly minimizes the empirical error in factual outcomes and the uncertainty in (unobserved) counterfactual outcomes. We conduct experiments on observational datasets for an interventional social program applied to premature infants, and a left ventricular assist device applied to cardiac patients wait-listed for a heart transplant. In both experiments, we show that our method significantly outperforms the state-of-the-art.
Intelligent agents are often faced with the need to choose actions with uncertain consequences, and to modify those actions according to ongoing sensory processing and changing task demands. The requisite ability to dynamically modify or cancel planned actions is known as inhibitory control in psychology. We formalize inhibitory control as a rational decision-making problem, and apply to it to the classical stop-signal task. Using Bayesian inference and stochastic control tools, we show that the optimal policy systematically depends on various parameters of the problem, such as the relative costs of different action choices, the noise level of sensory inputs, and the dynamics of changing environmental demands. Our normative model accounts for a range of behavioral data in humans and animals in the stop-signal task, suggesting that the brain implements statistically optimal, dynamically adaptive, and reward-sensitive decision-making in the context of inhibitory control problems.
We introduce the Gamma-Exponential Process (GEP), a prior over a large family ofcontinuous time stochastic processes. A hierarchical version of this prior (HGEP; the Hierarchical GEP) yields a useful model for analyzing complex time series. Models based on HGEPs display many attractive properties: conjugacy, exchangeability and closed-form predictive distribution for the waiting times, and exact Gibbs updates for the time scale parameters. After establishing these properties, weshow how posterior inference can be carried efficiently using Particle MCMC methods . This yields a MCMC algorithm that can resample entire sequences atomicallywhile avoiding the complications of introducing slice and stick auxiliary variables of the beam sampler . We applied our model to the problem of estimating the disease progression in multiple sclerosis , and to RNA evolutionary modeling. In both domains, we found that our model outperformed the standard rate matrix estimation approach.