LGAIMLMay 11, 2016

A constrained L1 minimization approach for estimating multiple Sparse Gaussian or Nonparanormal Graphical Models

arXiv:1605.03468v612 citations
AI Analysis

This work addresses the need for identifying context-specific networks in fields like bioinformatics and neuroimaging, offering a novel approach that is incremental in improving multi-graph estimation methods.

The authors tackled the problem of jointly estimating multiple sparse undirected graphical models from aggregated data across different contexts, proposing SIMULE to automatically infer both shared and context-specific edge patterns. The method achieved a consistent result at a rate of O(log(Kp)/n_tot) and showed significant improvement over state-of-the-art baselines on synthetic and biomedical datasets.

Identifying context-specific entity networks from aggregated data is an important task, arising often in bioinformatics and neuroimaging. Computationally, this task can be formulated as jointly estimating multiple different, but related, sparse Undirected Graphical Models (UGM) from aggregated samples across several contexts. Previous joint-UGM studies have mostly focused on sparse Gaussian Graphical Models (sGGMs) and can't identify context-specific edge patterns directly. We, therefore, propose a novel approach, SIMULE (detecting Shared and Individual parts of MULtiple graphs Explicitly) to learn multi-UGM via a constrained L1 minimization. SIMULE automatically infers both specific edge patterns that are unique to each context and shared interactions preserved among all the contexts. Through the L1 constrained formulation, this problem is cast as multiple independent subtasks of linear programming that can be solved efficiently in parallel. In addition to Gaussian data, SIMULE can also handle multivariate Nonparanormal data that greatly relaxes the normality assumption that many real-world applications do not follow. We provide a novel theoretical proof showing that SIMULE achieves a consistent result at the rate O(log(Kp)/n_{tot}). On multiple synthetic datasets and two biomedical datasets, SIMULE shows significant improvement over state-of-the-art multi-sGGM and single-UGM baselines.

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