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Bayesian correlated clustering to integrate multiple datasets. | LitMetric

AI Article Synopsis

  • The integration of multiple datasets in systems biology is crucial, and the authors propose a Bayesian method called MDI (Multiple Dataset Integration) that can handle diverse data types, including time series data.
  • MDI uses a Dirichlet-multinomial allocation (DMA) mixture model to analyze the relationships between datasets and measures how well they align with one another.
  • The method shows promising results by effectively integrating various datasets, including those related to gene expression and protein interaction, and outperforms existing techniques in identifying co-regulated protein complexes during the cell cycle.

Article Abstract

Motivation: The integration of multiple datasets remains a key challenge in systems biology and genomic medicine. Modern high-throughput technologies generate a broad array of different data types, providing distinct-but often complementary-information. We present a Bayesian method for the unsupervised integrative modelling of multiple datasets, which we refer to as MDI (Multiple Dataset Integration). MDI can integrate information from a wide range of different datasets and data types simultaneously (including the ability to model time series data explicitly using Gaussian processes). Each dataset is modelled using a Dirichlet-multinomial allocation (DMA) mixture model, with dependencies between these models captured through parameters that describe the agreement among the datasets.

Results: Using a set of six artificially constructed time series datasets, we show that MDI is able to integrate a significant number of datasets simultaneously, and that it successfully captures the underlying structural similarity between the datasets. We also analyse a variety of real Saccharomyces cerevisiae datasets. In the two-dataset case, we show that MDI's performance is comparable with the present state-of-the-art. We then move beyond the capabilities of current approaches and integrate gene expression, chromatin immunoprecipitation-chip and protein-protein interaction data, to identify a set of protein complexes for which genes are co-regulated during the cell cycle. Comparisons to other unsupervised data integration techniques-as well as to non-integrative approaches-demonstrate that MDI is competitive, while also providing information that would be difficult or impossible to extract using other methods.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3519452PMC
http://dx.doi.org/10.1093/bioinformatics/bts595DOI Listing

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