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.