4.8 Article

Quantification of Differential Transcription Factor Activity and Multiomics-Based Classification into Activators and Repressors: diffTF

Journal

CELL REPORTS
Volume 29, Issue 10, Pages 3147-+

Publisher

CELL PRESS
DOI: 10.1016/j.celrep.2019.10.106

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Funding

  1. EMBL
  2. Fundacion Ramon Areces
  3. Otto Bayer Scholarship from Bayer Foundations
  4. Danish Medical Research Council [FSS 1333-00120B]
  5. Independent Research Fund Denmark [8020-00044B]
  6. European Research Council [294666_DNAMET]
  7. Novo Nordisk Foundation [NNF17CC0027852]
  8. Memorial Sloan Kettering Cancer Center [NIH P30 CA008748]

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Transcription factors (TFs) regulate many cellular processes and can therefore serve as readouts of the signaling and regulatory state. Yet for many TFs, the mode of action-repressing or activating transcription of target genes-is unclear. Here, we present diffTF (https://git.embl.de/grp-zaugg/diffTF) to calculate differential TF activity (basic mode) and classify TFs into putative transcriptional activators or repressors (classification mode). In basic mode, it combines genome-wide chromatin accessibility/activity with putative TF binding sites that, in classification mode, are integrated with RNA-seq. We apply diffTF to compare (1) mutated and unmutated chronic lymphocytic leukemia patients and (2) two hematopoietic progenitor cell types. In both datasets, diffTF recovers most known biology and finds many previously unreported TFs. It classifies almost 40% of TFs based on their mode of action, which we validate experimentally. Overall, we demonstrate that diffTF recovers known biology, identifies less well-characterized TFs, and classifies TFs into transcriptional activators or repressors.

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