TFTA

TFTA quantifies collective transcriptional activation of transcription factor target genes to detect and analyze altered transcription factor activity in cancer.


Key Features:

  • Detection of Perturbed Regulators: Identifies transcription factors with altered activity in cancerous tissues compared to normal tissues.
  • Large-Scale Application: Applied to 5,607 cancer samples across eleven different types of cancer to assess TF activity at scale.
  • Comprehensive Catalogue Creation: Produces a catalogue detailing altered transcription factor activities across multiple cancers.
  • Association with Patient Survival: Reveals associations between specific TF activities and patient survival outcomes.
  • Identification of Prognostic TFs: Detects transcription factors whose activity remains relatively unchanged between cancer and normal tissues but correlates with prognosis.
  • Personalized TF Activity Estimates: Provides per-patient estimates of transcription factor activity for individualized analysis.

Scientific Applications:

  • Cancer Research and Diagnosis: Characterizes TF regulatory perturbations to inform molecular understanding and potential diagnostic markers.
  • Therapeutic Target Identification: Prioritizes transcription factors with prognostic relevance as candidate therapeutic targets.
  • Personalized Treatment Strategies: Supports individualized molecular profiling by supplying patient-specific TF activity estimates.

Methodology:

Quantifies the collective transcriptional activation of target genes regulated by specific transcription factors and leverages large-scale cancer datasets to detect TF activity changes that may be subtle relative to traditional gene expression analyses.

Topics

Details

Tool Type:
command-line tool
Operating Systems:
Mac, Linux, Windows
Programming Languages:
R
Added:
3/23/2022
Last Updated:
3/23/2022

Operations

Publications

Falco MM, Bleda M, Carbonell-Caballero J, Dopazo J. The pan-cancer pathological regulatory landscape. Scientific Reports. 2016;6(1). doi:10.1038/srep39709. PMID:28000771. PMCID:PMC5175166.

Documentation

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