4.8 Article

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

期刊

MOLECULAR CELL
卷 28, 期 2, 页码 337-350

出版社

CELL PRESS
DOI: 10.1016/j.molcel.2007.09.027

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资金

  1. NHGRI NIH HHS [R01 HG003219, R01 HG003219-04] Funding Source: Medline
  2. NIGMS NIH HHS [P50 GM071508] Funding Source: Medline

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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 cooccurrences of DNA and RNA motifs, context dependent selection for motif avoidance, and the strong impact of post transcriptional processes on eukaryotic transcriptomes.

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