disease network
Higher order organizational features can distinguish protein interaction networks of disease classes: a case study of neoplasms and neurological diseases
Neoplasms (NPs) and neurological diseases and disorders (NDDs) are amongst the major classes of diseases underlying deaths of a disproportionate number of people worldwide. To determine if there exist some distinctive features in the local wiring patterns of protein interactions emerging at the onset of a disease belonging to either of these two classes, we examined 112 and 175 protein interaction networks belonging to NPs and NDDs, respectively. Orbit usage profiles (OUPs) for each of these networks were enumerated by investigating the networks' local topology. 56 non-redundant OUPs (nrOUPs) were derived and used as network features for classification between these two disease classes. Four machine learning classifiers, namely, k-nearest neighbour (KNN), support vector machine (SVM), deep neural network (DNN), random forest (RF) were trained on these data. DNN obtained the greatest average AUPRC (0.988) among these classifiers. DNNs developed on node2vec and the proposed nrOUPs embeddings were compared using 5-fold cross validation on the basis of average values of the six of performance measures, viz., AUPRC, Accuracy, Sensitivity, Specificity, Precision and MCC. It was found that nrOUPs based classifier performed better in all of these six performance measures.
- Asia > India (0.05)
- South America > Chile > Santiago Metropolitan Region > Santiago Province > Santiago (0.04)
- Health & Medicine > Pharmaceuticals & Biotechnology (1.00)
- Health & Medicine > Therapeutic Area > Neurology (0.85)
Learning Dynamic and Personalized Comorbidity Networks from Event Data using Deep Diffusion Processes
Qian, Zhaozhi, Alaa, Ahmed M., Bellot, Alexis, Rashbass, Jem, van der Schaar, Mihaela
Comorbid diseases cooccur and progress via complex temporal patterns that vary among individuals. In electronic health records we can observe the different diseases a patient has, but can only infer the temporal relationship between each co-morbid condition. Learning such temporal patterns from event data is crucial for understanding disease pathology and predicting prognoses. To this end, we develop deep diffusion processes (DDP) to model "dynamic comorbid-ity networks", i.e., the temporal relationships between comorbid disease onsets expressed through a dynamic graph. A DDP comprises events modelled as a multidimensional point process, with an intensity function parame-terized by the edges of a dynamic weighted graph. The graph structure is modulated by a neural network that maps patient history to edge weights, enabling rich temporal representations for disease trajectories. The DDP parameters decouple into clinically meaningful components, which enables serving the dual purpose of accurate risk prediction and intelligible representation of disease pathology. We illustrate these features in experiments using cancer registry data.
- Europe > United Kingdom > England > Cambridgeshire > Cambridge (0.04)
- Europe > Italy > Sicily > Palermo (0.04)
- Research Report > Experimental Study (0.68)
- Research Report > New Finding (0.46)
- Health & Medicine > Therapeutic Area > Oncology (1.00)
- Health & Medicine > Therapeutic Area > Cardiology/Vascular Diseases (1.00)
- Health & Medicine > Consumer Health (0.95)
- Health & Medicine > Therapeutic Area > Gastroenterology (0.95)
Precision disease networks (PDN)
Cabrera, J., Amaratunga, D., Kostis, W., Kostis, J
The a rrows represent the frequency of the relationship from A to B i n the cluster of pa tients, R ed arrows repre sente a frequency of 75% or more of the cluster observations containinig the relation ship, green arrows repre sent a frequency in the range 50% - 75%, whereas yellow arrows repre sent repre sent a frequency in the range 25% - 50%. For step 3 we performed a hierarchical cluster analysis using the WARD method that resulted in 10 clust ers for each of the 4 PCA datasets. Figure 2 shows a scatter plot of the first two components of the first of the cluster analysis where the 10 clusters are shown in different colors. In Figure 3 we display the summaries of the 10 clusters. For step 4 we used the cox proportional hazard model with the variable "all death" as response that measures the date of death for any cause of death. We fitted 7 different models using different combinations of predictors as shown on table 1.
- North America > United States > New Jersey (0.06)
- North America > United States > New York (0.05)
Learning Hawkes Processes from Short Doubly-Censored Event Sequences
Xu, Hongteng, Luo, Dixin, Zha, Hongyuan
Many real-world applications require robust algorithms to learn point processes based on a type of incomplete data --- the so-called short doubly-censored (SDC) event sequences. We study this critical problem of quantitative asynchronous event sequence analysis under the framework of Hawkes processes by leveraging the idea of data synthesis. Given SDC event sequences observed in a variety of time intervals, we propose a sampling-stitching data synthesis method --- sampling predecessors and successors for each SDC event sequence from potential candidates and stitching them together to synthesize long training sequences. The rationality and the feasibility of our method are discussed in terms of arguments based on likelihood. Experiments on both synthetic and real-world data demonstrate that the proposed data synthesis method improves learning results indeed for both time-invariant and time-varying Hawkes processes.
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- Oceania > Australia > New South Wales > Sydney (0.04)
- Asia > Middle East > Israel (0.04)
- Asia > China > Shanghai > Shanghai (0.04)
- Information Technology > Communications > Social Media (1.00)
- Information Technology > Artificial Intelligence > Machine Learning (1.00)
- Information Technology > Data Science (0.93)