rSeqTU-A

rSeqTU-A predicts bacterial transcription units (TUs) from RNA-seq data using machine learning to delineate co-transcribed adjacent genes in prokaryotic genomes.


Key Features:

  • Implementation: Implemented as an R package.
  • Machine Learning Integration: Uses random forest for feature selection (including gene intergenic distance and continuous RNA-seq read count signals) and support vector machines (SVM) to build TU prediction models.
  • Comprehensive Pipeline: Provides end-to-end processing including quality control of reads, read mapping, training set generation, feature selection, TU prediction, and visualization.
  • Computational Compatibility: Supports execution on local computers and high-performance clusters.
  • Enhanced Visualization Tools: Includes functionalities for visualizing predicted transcription units.

Scientific Applications:

  • Transcriptional regulatory network analysis: Delineates transcriptional regulatory networks and dynamic regulatory mechanisms in prokaryotic genomes.
  • Microbial genomics: Identifies co-transcribed gene clusters (TUs) to support genome annotation and comparative genomics.
  • Transcriptomics: Facilitates interpretation of RNA-seq data to infer transcriptional organization.
  • Systems biology: Provides TU-level information to inform systems biology models of bacterial gene regulation.

Methodology:

Performs quality control of reads, read mapping, training set generation, random forest-based feature selection using genomic (gene intergenic distance) and transcriptomic (continuous RNA-seq read count signals) features, and constructs support vector machine (SVM) models for TU prediction.

Topics

Details

License:
MIT
Maturity:
Mature
Cost:
Free of charge
Tool Type:
library
Operating Systems:
Linux, Windows, Mac
Programming Languages:
R
Added:
6/20/2019
Last Updated:
6/16/2020

Operations

Publications

Niu S, Liu B, Ma Q, Chou W. rSeqTU—A Machine-Learning Based R Package for Prediction of Bacterial Transcription Units. Frontiers in Genetics. 2019;10. doi:10.3389/fgene.2019.00374. PMID:31156694. PMCID:PMC6529933.

PMID: 31156694
PMCID: PMC6529933
Funding: - National Science Foundation: #ACI-1548562

Documentation