Bioinformatics AdvancesBioinformaticsPeer-reviewed journal article
Improving confidence of differential transcription calls in enhancers
Hope A. TownsendiD, Jacob T. StanleyiD, Mary Ann AlleniD, Robin D. DowelliD
Abstract
MotivationMost disease-associated genetic variants reside within transcribed regulatory elements (tREs). Patterns of differential transcription at tREs can be leveraged to identify upstream regulators and link enhancers to their target genes. But the low transcription levels and high variability in tREs makes identifying high confidence differentially transcribed elements challenging. ResultsWe present Mu Counts and TFEA-LE, two algorithms for robust identification of differentially transcribed tREs. The first step in accurate identification of differentially transcribed tREs is to obtain accurate RNA lengths and therefore counts over these regions. To this end we developed a method of accurate length inference (LIET-EMG) as wll as a rapid method for counting reads over tREs (Mu Counts). Armed with newly identified and quantified tREs, TFEA-LE then integrates motif information to simultaneously identify responsive tREs and their likely upstream regulators. We show improved precision and recall over general-purpose tools (e.g. DESeq2) in detecting p53-responsive tREs. We then clarify TF-specific responses within multi-TF perturbations in lung cells. Finally we show that the TFEA-LE approach improves TF activity inference, including in complex perturbations where many TFs respond. TFEALE is especially effective in technically challenging datasets, whether due to highly specific or broad responses, outliers, or high GC content. Ultimately, these 1 methods advance the systematic characterization of individual tREs, enabling their integration with regulators, target genes, and disease-associated variants for translational research. Availability and ImplementationTFEA-LE: https://github.com/Dowell-Lab/TFEA/tree/Lead_edge. Nextflow pipeline to run Mu Counts: https://github.com/Dowell-Lab/Bidir_Counting_Analysis. LIET (including modifications for tREs): https://github.com/Dowell-Lab/LIET/tree/LIET_EMGtoo. Source code for this work: https://github.com/Dowell-Lab/Improving_tRE_Analysis_Paper Contactrobin.dowell@colorado.edu
- organism: human
- assay: bulk RNA-seq
- research focus: differential expression
- research focus: gene regulatory network inference
- research focus: benchmarking
- research focus: database / resource
- approach: statistical model
- approach: machine learning (classical)
- Citations
- 0
- FWCI
- 0.00
- Field percentile
- 33th percentile
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- Transcription factor enrichment analysis (TFEA): Quantifying the activity of hundreds of transcription factors from a single experiment
Jonathan D. Rubin, Jacob T. Stanley, … Robin D. Dowell·Communications BiologyPeer-reviewed·Jun 2, 2021
- Enhancing TFEA.ChIP with ENCODE Regulatory Maps for Generalizable Transcription Factor Enrichment
Yosra Berrouayel, Luis del Peso·Briefings in BioinformaticsPeer-reviewed·Jan 1, 2026
- Accurate differential analysis of transcription factor activity from gene expression
Viren R. Amin, Didem Ağaç Çobanoğlu, … Murat Can Çobanoğlu·BioinformaticsPeer-reviewed·May 8, 2019
- TFEA.ChIP: A tool kit for transcription factor binding site enrichment analysis capitalizing on ChIP-seq datasets
Laura Puente-Santamaría, Wyeth W. Wasserman, Luis del Peso·BioinformaticsPeer-reviewed·Jul 24, 2019
- Accurate Identification of Active Transcriptional Regulatory Elements from Global Run-On and Sequencing Data
Charles G Danko, Stephanie L Hyland, … Adam Siepel·bioRxiv·Nov 12, 2014
- TF-Prioritizer: a java pipeline to prioritize condition-specific transcription factors
Markus Hoffmann, Nico Trummer, … Markus List·GigaSciencePeer-reviewed·Dec 28, 2022