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      A universal framework for regulatory element discovery across all genomes and data types.

      Molecular Cell

      Untranslated Regions, Animals, Cluster Analysis, DNA, Fungal, chemistry, metabolism, DNA, Protozoan, Databases, Genetic, Gene Expression Profiling, Gene Expression Regulation, Gene Expression Regulation, Fungal, Humans, Mice, MicroRNAs, Nucleic Acid Conformation, Oligonucleotide Array Sequence Analysis, Plasmodium falciparum, genetics, RNA, Fungal, RNA, Protozoan, Regulatory Elements, Transcriptional, Regulatory Sequences, Nucleic Acid, Reproducibility of Results, Saccharomyces cerevisiae, Sequence Analysis, DNA, methods, Sequence Analysis, RNA, Sequence Homology, Nucleic Acid, Software, Time Factors, Transcription Factors

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          Abstract

          Deciphering the noncoding regulatory genome has proved a formidable challenge. Despite the wealth of available gene expression data, there currently exists no broadly applicable method for characterizing the regulatory elements that shape the rich underlying dynamics. We present a general framework for detecting such regulatory DNA and RNA motifs that relies on directly assessing the mutual information between sequence and gene expression measurements. Our approach makes minimal assumptions about the background sequence model and the mechanisms by which elements affect gene expression. This provides a versatile motif discovery framework, across all data types and genomes, with exceptional sensitivity and near-zero false-positive rates. Applications from yeast to human uncover putative and established transcription-factor binding and miRNA target sites, revealing rich diversity in their spatial configurations, pervasive co-occurrences of DNA and RNA motifs, context-dependent selection for motif avoidance, and the strong impact of posttranscriptional processes on eukaryotic transcriptomes.

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          Author and article information

          Journal
          17964271
          2900317
          10.1016/j.molcel.2007.09.027

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