4.7 Article

Measurement of genome-wide RNA synthesis and decay rates with Dynamic Transcriptome Analysis (DTA)

Journal

BIOINFORMATICS
Volume 28, Issue 6, Pages 884-885

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/bioinformatics/bts052

Keywords

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Funding

  1. LMUexcellent guest professorship
  2. Deutsche Forschungsgemeinschaft [SFB646, TR5, FOR1068]
  3. NIM
  4. European Molecular Biology Organization (EMBO)
  5. European Research Council
  6. LMUinnovativ project Bioimaging Network (BIN)
  7. Jung-Stiftung

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Standard transcriptomics measures total cellular RNA levels. Our understanding of gene regulation would be greatly improved if we could measure RNA synthesis and decay rates on a genome-wide level. To that end, the Dynamic Transcriptome Analysis (DTA) method has been developed. DTA combines metabolic RNA labeling with standard transcriptomics to measure RNA synthesis and decay rates in a precise and non-perturbing manner. Here, we present the open source R/Bioconductor software package DTA. It implements all required bioinformatics steps that allow the accurate absolute quantification and comparison of RNA turnover.

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