Correlation Engine 2.0
Clear Search sequence regions


  • cell (3)
  • chromatin (2)
  • chromosome (1)
  • consistency (1)
  • dna (1)
  • gene (2)
  • human (2)
  • human cell (3)
  • nucleic acids (1)
  • organ specificity (1)
  • regions (1)
  • research (2)
  • Sizes of these terms reflect their relevance to your search.

    The Roadmap Epigenomics Consortium has published whole-genome functional annotation maps in 127 human cell types by integrating data from studies of multiple epigenetic marks. These maps have been widely used for studying gene regulation in cell type-specific contexts and predicting the functional impact of DNA mutations on disease. Here, we present a new map of functional elements produced by applying a method called IDEAS on the same data. The method has several unique advantages and outperforms existing methods, including that used by the Roadmap Epigenomics Consortium. Using five categories of independent experimental datasets, we compared the IDEAS and Roadmap Epigenomics maps. While the overall concordance between the two maps is high, the maps differ substantially in the prediction details and in their consistency of annotation of a given genomic position across cell types. The annotation from IDEAS is uniformly more accurate than the Roadmap Epigenomics annotation and the improvement is substantial based on several criteria. We further introduce a pipeline that improves the reproducibility of functional annotation maps. Thus, we provide a high-quality map of candidate functional regions across 127 human cell types and compare the quality of different annotation methods in order to facilitate biomedical research in epigenomics. © The Author(s) 2017. Published by Oxford University Press on behalf of Nucleic Acids Research.

    Citation

    Yu Zhang, Ross C Hardison. Accurate and reproducible functional maps in 127 human cell types via 2D genome segmentation. Nucleic acids research. 2017 Sep 29;45(17):9823-9836

    Expand section icon Mesh Tags

    Expand section icon Substances


    PMID: 28973456

    View Full Text