Abstract

Enormous amounts of biomedical data have been and are being produced by investigators all over the world. However, one crucial and limiting factor in data reuse is accurate, structured and complete description of the data or data about the data—defined as metadata. We propose a framework to predict structured metadata terms from unstructured metadata for improving quality and quantity of metadata, using the Gene Expression Omnibus (GEO) microarray database. Our framework consists of classifiers trained using term frequency-inverse document frequency (TF-IDF) features and a second approach based on topics modeled using a Latent Dirichlet Allocation model (LDA) to reduce the dimensionality of the unstructured data. Our results on the GEO database show that structured metadata terms can be the most accurately predicted using the TF-IDF approach followed by LDA both outperforming the majority vote baseline. While some accuracy is lost by the dimensionality reduction of LDA, the difference is small for elements with few possible values, and there is a large improvement over the majority classifier baseline. Overall this is a promising approach for metadata prediction that is likely to be applicable to other datasets and has implications for researchers interested in biomedical metadata curation and metadata prediction.Database URL: http://www.yeastgenome.org/

Highlights

  • Enormous amounts of biomedical data have been and are being produced by investigators all over the world

  • Several databases were created in the process to house this data and make it available to the community at large, such as the NCBI databases for microarray data; Gene Expression Omnibus (GEO) [1] and sequence data; the VC The Author(s) 2016

  • The main contribution of this paper is to explore whether unstructured gene expression sample metadata contains information, which can be exploited for predicting structured metadata using traditional text mining methods based on term frequency-inverse document frequency (TF-IDF)

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Summary

Introduction

Enormous amounts of biomedical data have been and are being produced by investigators all over the world. This is mainly due to advancements in molecular technologies that have enabled extensive profiling of biological samples and have unleashed a myriad of omics data such as gene expression, microRNA expression, DNA methylation and DNA mutation data. Realized that this data should be stored and shared with other investigators.

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