We will review some of the major results in random graphs and some of the more challenging open problems. We will cover algorithmic and structural questions. We will touch on newer models, including those related to the WWW.

Random graphs

https://spiral.imperial.ac.uk/bitstream/10044/1/71213/5/1-s2.0-S1074761318301213-main.pdf

The Immune Landscape of Cancer

https://minerva-access.unimelb.edu.au/bitstream/handle/11343/253538/PMC5957518.pdf

Cell-of-Origin Patterns Dominate the Molecular Classification of 10,000 Tumors from 33 Types of Cancer.

Single-cell transcriptomics allows researchers to investigate complex communities of heterogeneous cells. It can be applied to stem cells and their descendants in order to chart the progression from multipotent progenitors to fully differentiated cells. While a variety of statistical and computational methods have been proposed for inferring cell lineages, the problem of accurately characterizing multiple branching lineages remains difficult to solve. We introduce Slingshot, a novel method for inferring cell lineages and pseudotimes from single-cell gene expression data. In previously published datasets, Slingshot correctly identifies the biological signal for one to three branching trajectories. Additionally, our simulation study shows that Slingshot infers more accurate pseudotimes than other leading methods. Slingshot is a uniquely robust and flexible tool which combines the highly stable techniques necessary for noisy single-cell data with the ability to identify multiple trajectories. Accurate lineage inference is a critical step in the identification of dynamic temporal gene expression.

/pdf/slingshot-cell-lineage-and-pseudotime-inference-for-single-2xc55fkwkf.pdf

Slingshot: cell lineage and pseudotime inference for single-cell transcriptomics

8. Subset Selection in Regression (Monographs on Statistics and Applied Probability, no. 40). By A. J. Miller. ISBN 0 412 35380 6. Chapman and Hall, London, 1990. 240 pp. £25.00.

Subset Selection in Regression

Finite mixture models are being used increasingly to model a wide variety of random phenomena for clustering, classification and density estimation. mclust is a powerful and popular package which allows modelling of data as a Gaussian finite mixture with different covariance structures and different numbers of mixture components, for a variety of purposes of analysis. Recently, version 5 of the package has been made available on CRAN. This updated version adds new covariance structures, dimension reduction capabilities for visualisation, model selection criteria, initialisation strategies for the EM algorithm, and bootstrap-based inference, making it a full-featured R package for data analysis via finite mixture modelling.

https://researchrepository.ucd.ie/bitstream/10197/7937/1/insight_publication.pdf

mclust 5: Clustering, Classification and Density Estimation Using Gaussian Finite Mixture Models.

Model-based clustering is a popular approach for clustering multivariate data which has seen applications in numerous fields. Nowadays, high-dimensional data are more and more common and the model-based clustering approach has adapted to deal with the increasing dimensionality. In particular, the development of variable selection techniques has received a lot of attention and research effort in recent years. Even for small size problems, variable selection has been advocated to facilitate the interpretation of the clustering results. This review provides a summary of the methods developed for variable selection in model-based clustering. Existing R packages implementing the different methods are indicated and illustrated in application to two data analysis examples.

Variable Selection Methods for Model-based Clustering

/pdf/variable-selection-methods-for-model-based-clustering-4ofpxtrln8.pdf

Variable selection methods for model-based clustering

The identification of most relevant clinical criteria related to low back pain disorders may aid the evaluation of the nature of pain suffered in a way that usefully informs patient assessment and treatment. Data concerning low back pain can be of categorical nature, in the form of a check-list in which each item denotes presence or absence of a clinical condition. Latent class analysis is a model-based clustering method for multivariate categorical responses, which can be applied to such data for a preliminary diagnosis of the type of pain. In this work, we propose a variable selection method for latent class analysis applied to the selection of the most useful variables in detecting the group structure in the data. The method is based on the comparison of two different models and allows the discarding of those variables with no group information and those variables carrying the same information as the already selected ones. We consider a swap-stepwise algorithm where at each step the models are compared through an approximation to their Bayes factor. The method is applied to the selection of the clinical criteria most useful for the clustering of patients in different classes. It is shown to perform a parsimonious variable selection and to give a clustering performance comparable to the expert-based classification of patients into three classes of pain.

Variable Selection for Latent Class Analysis with Application to Low Back Pain Diagnosis

Finite Gaussian mixture models are widely used for model-based clustering of continuous data. Nevertheless, since the number of model parameters scales quadratically with the number of variables, these models can be easily over-parameterized. For this reason, parsimonious models have been developed via covariance matrix decompositions or assuming local independence. However, these remedies do not allow for direct estimation of sparse covariance matrices nor do they take into account that the structure of association among the variables can vary from one cluster to the other. To this end, we introduce mixtures of Gaussian covariance graph models for model-based clustering with sparse covariance matrices. A penalized likelihood approach is employed for estimation and a general penalty term on the graph configurations can be used to induce different levels of sparsity and incorporate prior knowledge. Model estimation is carried out using a structural-EM algorithm for parameters and graph structure estimation, where two alternative strategies based on a genetic algorithm and an efficient stepwise search are proposed for inference. With this approach, sparse component covariance matrices are directly obtained. The framework results in a parsimonious model-based clustering of the data via a flexible model for the within-group joint distribution of the variables. Extensive simulated data experiments and application to illustrative datasets show that the method attains good classification performance and model quality. The general methodology for model-based clustering with sparse covariance matrices is implemented in the R package mixggm, available on CRAN.

/pdf/model-based-clustering-with-sparse-covariance-matrices-1fw8h1kp50.pdf

Michael Fop

Papers

mclust 5: Clustering, Classification and Density Estimation Using Gaussian Finite Mixture Models.

Variable Selection Methods for Model-based Clustering

Variable selection methods for model-based clustering

Variable Selection for Latent Class Analysis with Application to Low Back Pain Diagnosis

Model-based clustering with sparse covariance matrices