TrawlerWeb

TrawlerWeb performs de novo motif discovery and predicts transcription factor binding site (TFBS) composition from DNA sequences derived from next-generation sequencing (NGS) experiments.


Key Features:

  • De novo motif discovery: Performs de novo motif discovery on input DNA sequences.
  • TFBS composition prediction: Predicts transcription factor binding site (TFBS) composition for identified motifs.
  • NGS input (BED): Accepts BED files generated from NGS experiments as input.
  • Input-matched biological background: Automatically generates input-matched biological background sequences for enrichment analysis.
  • Conservation scores: Reports conservation scores for each identified motif instance to aid prioritization.
  • Performance: Provides a fast motif-discovery implementation suitable for large NGS-derived datasets.

Scientific Applications:

  • Transcriptional regulation analysis: Identify enriched motifs and predict TFBS composition to study gene regulation mechanisms.
  • Regulatory element discovery: Detect novel cis-regulatory elements in non-coding genomic regions from NGS data.
  • Experimental prioritization: Prioritize motif instances for experimental validation using reported conservation scores.

Methodology:

Performs de novo motif discovery on DNA sequences (BED input from NGS), generates an input-matched biological background, identifies enriched motifs, assigns conservation scores to motif instances, and predicts TFBS composition.

Topics

Details

License:
GPL-3.0
Tool Type:
command-line tool, web application
Operating Systems:
Linux, Windows, Mac
Programming Languages:
Java, Perl
Added:
7/25/2018
Last Updated:
12/10/2018

Operations

Publications

Dang LT, Tondl M, Chiu MHH, Revote J, Paten B, Tano V, Tokolyi A, Besse F, Quaife-Ryan G, Cumming H, Drvodelic MJ, Eichenlaub MP, Hallab JC, Stolper JS, Rossello FJ, Bogoyevitch MA, Jans DA, Nim HT, Porrello ER, Hudson JE, Ramialison M. TrawlerWeb: an online de novo motif discovery tool for next-generation sequencing datasets. BMC Genomics. 2018;19(1). doi:10.1186/s12864-018-4630-0. PMID:29621972. PMCID:PMC5887194.

PMID: 29621972
PMCID: PMC5887194
Funding: - Australian Research Council: DP1049980 - National Health and Medical Research Council: 1049980

Documentation