TSSer
TSSer identifies transcription start sites (TSSs) genome-wide in bacterial genomes from differential RNA sequencing (dRNA-seq) data using a probabilistic framework to infer TSS positions for studies of bacterial transcription initiation and regulation.
Key Features:
- Probabilistic framework: Uses a probabilistic model to automatically infer TSSs from dRNA-seq signal.
- dRNA-seq analysis: Operates on differential RNA sequencing (dRNA-seq) datasets to detect transcription initiation sites.
- Genome-wide mapping: Performs genome-wide identification of TSSs in bacterial genomes.
- Enrichment detection: Identifies genomic positions preferentially enriched in dRNA-seq data.
- Capture-preference analysis: Detects positions preferentially captured relative to neighboring regions to refine TSS calls.
- Validation and discovery: Demonstrates high consistency with curated TSS lists and uncovers additional TSSs using publicly available datasets.
- Automated inference: Automates the computational inference of TSSs from sequencing data.
Scientific Applications:
- Genome-wide TSS annotation: Generate comprehensive TSS maps for bacterial genomes from dRNA-seq data.
- Transcriptional regulatory network analysis: Provide TSS locations to support studies of bacterial gene regulation and promoter architecture.
- Comparative and validation studies: Compare inferred TSSs with curated lists and publicly available datasets to identify novel transcription start sites.
Methodology:
TSSer applies a probabilistic framework to dRNA-seq data to identify genomic positions that are preferentially enriched and preferentially captured relative to neighboring regions and compares results to publicly available datasets and curated TSS lists.
Topics
Details
- Tool Type:
- command-line tool
- Operating Systems:
- Linux, Windows, Mac
- Added:
- 8/3/2017
- Last Updated:
- 11/25/2024
Operations
Publications
Jorjani H, Zavolan M. TSSer: an automated method to identify transcription start sites in prokaryotic genomes from differential RNA sequencing data. Bioinformatics. 2013;30(7):971-974. doi:10.1093/bioinformatics/btt752. PMID:24371151.