NPLB
NPLB characterizes promoter architectures from genome-wide transcription start site (TSS) data to analyze promoter diversity and regulatory structures across organisms.
Key Features:
- Organism-Independent Analysis: Analyzes promoter architectures across different species using genome-wide TSS data.
- Direct Characterization from TSSs: Characterizes promoter architectures directly from experimentally identified genome-wide TSSs without requiring predefined promoter elements.
- Identification of Novel Architectures: Identifies novel promoter architectures, as demonstrated by discovery of previously unrecognized structures in the fly genome.
Scientific Applications:
- Promoter Diversity and Function: Elucidates promoter diversity and functional promoter classes in genomic research.
- Gene Regulation Mechanisms: Supports studies of gene regulation mechanisms by identifying promoter structures associated with transcriptional outcomes.
- Comparative and Evolutionary Genomics: Enables comparative and evolutionary genomics analyses by comparing promoter architectures across organisms.
Methodology:
Analyzes experimentally identified genome-wide TSSs and characterizes promoter architectures without relying on predefined promoter elements, including detection of promoters with or without canonical features such as the TATA-box.
Topics
Details
- Tool Type:
- web application
- Operating Systems:
- Linux, Windows, Mac
- Programming Languages:
- Python
- Added:
- 8/3/2017
- Last Updated:
- 11/25/2024
Operations
Publications
Mitra S, Narlikar L. No Promoter Left Behind (NPLB): learn <i>de novo</i> promoter architectures from genome-wide transcription start sites. Bioinformatics. 2015;32(5):779-781. doi:10.1093/bioinformatics/btv645. PMID:26530723. PMCID:PMC4795619.
Documentation
User manual
http://nplb.ncl.res.in/help.html