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BioGPS and GXD: mouse gene expression data—the benefits and challenges of data integration

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Abstract

Mouse gene expression data are complex and voluminous. To maximize the utility of these data, they must be made readily accessible through databases, and those resources need to place the expression data in the larger biological context. Here we describe two community resources that approach these problems in different but complementary ways: BioGPS and the Mouse Gene Expression Database (GXD). BioGPS connects its large and homogeneous microarray gene expression reference data sets via plugins with a heterogeneous collection of external gene centric resources, thus casting a wide but loose net. GXD acquires different types of expression data from many sources and integrates these data tightly with other types of data in the Mouse Genome Informatics (MGI) resource, with a strong emphasis on consistency checks and manual curation. We describe and contrast the “loose” and “tight” data integration strategies employed by BioGPS and GXD, respectively, and discuss the challenges and benefits of data integration. BioGPS is freely available at http://biogps.org. GXD is freely available through the MGI web site (www.informatics.jax.org) or directly at www.informatics.jax.org/expression.shtml.

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Acknowledgments

The authors thank Drs. Joel Richardson, Constance Smith, and Benjamin Good for their helpful comments and discussions on the manuscript. The authors also thank all the members of the GXD and BioGPS teams for their dedicated work, as well as the members of other MGI projects for their contributions to GXD and to the larger MGI Resource. The authors acknowledge support from the National Institute of General Medical Sciences (GM083924 to AIS) and from the Eunice Kennedy Shriver National Institute of Child Health and Human Development (HD062499 to MR).

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Correspondence to Martin Ringwald or Andrew I. Su.

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Ringwald, M., Wu, C. & Su, A.I. BioGPS and GXD: mouse gene expression data—the benefits and challenges of data integration. Mamm Genome 23, 550–558 (2012). https://doi.org/10.1007/s00335-012-9408-0

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  • DOI: https://doi.org/10.1007/s00335-012-9408-0

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