General Information
| Description | Robust multi-state identification of transcription factor binding sites from DNase-seq data |
| Homepage | http://github.com/ajank/Romulus |
Publications
Romulus: robust multi-state identification
of transcription factor binding sites from
DNase-seq data
Motivation:
Computational prediction of transcription factor (TF) binding sites in the genome remains a challenging task. Here, we present Romulus, a novel computational method for identifying individual TF binding sites from genome sequence information and cell-type–specific experimental data, such as DNase-seq. It combines the strengths of previous approaches, and improves robustness by reducing the number of free parameters in the model by an order of magnitude.
Results:
We show that Romulus significantly outperforms existing methods across three sources of DNase-seq data, by assessing the performance of these tools against ChIP-seq profiles. The difference was particularly significant when applied to binding site prediction for low-information-content motifs. Our method is capable of inferring multiple binding modes for a single TF, which differ in their DNase I cut profile. Finally, using the model learned by Romulus and ChIP-seq data, we introduce Binding in Closed Chromatin (BCC) as a quantitative measure of TF pioneer factor activity. Uniquely, our measure quantifies a defining feature of pioneer factors, namely their ability to bind closed chromatin.
Availability and Implementation:
Romulus is freely available as an R package at http://github.com/ajank/Romulus .
Contact:
ajank@mimuw.edu.pl
Supplementary information:
Supplementary data are available at Bioinformatics online.
FAIR Evaluation
Sorry, you must be signed in to evaluate this object.
