4.7 Article

annotatr: genomic regions in context

期刊

BIOINFORMATICS
卷 33, 期 15, 页码 2381-2383

出版社

OXFORD UNIV PRESS
DOI: 10.1093/bioinformatics/btx183

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资金

  1. Bioinformatics Training Grant (National Institute of General Medical Sciences) [T32 GM070499]
  2. National Cancer Institute [R01 CA158286]
  3. National Institute of Environmental Health Sciences [P30 ES017885]

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Motivation: Analysis of next-generation sequencing data often results in a list of genomic regions. These may include differentially methylated CpGs/regions, transcription factor binding sites, interacting chromatin regions, or GWAS-associated SNPs, among others. A common analysis step is to annotate such genomic regions to genomic annotations (promoters, exons, enhancers, etc.). Existing tools are limited by a lack of annotation sources and flexible options, the time it takes to annotate regions, an artificial one-to-one region-to-annotation mapping, a lack of visualization options to easily summarize data, or some combination thereof. Results: We developed the annotatr Bioconductor package to flexibly and quickly summarize and plot annotations of genomic regions. The annotatr package reports all intersections of regions and annotations, giving a better understanding of the genomic context of the regions. A variety of graphics functions are implemented to easily plot numerical or categorical data associated with the regions across the annotations, and across annotation intersections, providing insight into how characteristics of the regions differ across the annotations. We demonstrate that annotatr is up to 27x faster than comparable R packages. Overall, annotatr enables a richer biological interpretation of experiments.

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