NPACT
NPACT identifies and quantitatively characterizes sequence regions exhibiting three-base compositional periodicity indicative of open reading frames (ORFs).
Key Features:
- Quantitative methodologies: Implements two novel quantitative methods to detect statistically significant 3-base compositional periodicities within nucleotide sequences.
- Frame-specific GC analysis: Quantitatively assesses GC usage variations across codon frame positions to reveal frame-dependent composition differences.
- Statistical characterization: Provides statistical assessment of identified periodicities and candidate ORF regions.
- Graphical representations: Produces graphical outputs that highlight contrasts in GC usage among codon frames and inconsistencies with existing coding-region annotations.
- High-GC genome application: Applies frame analysis to detect genes potentially missing from annotations in prokaryotic genomes with high GC content.
Scientific Applications:
- Genome annotation improvement: Identifies conserved and previously unrecognized ORFs to enhance completeness and accuracy of genome annotations.
- Analysis of high-GC prokaryotes: Detects candidate genes in high GC content prokaryotic genomes that may be overlooked by standard annotation methods.
- Case study application: Has been applied to two strains of the deltaproteobacterium Anaeromyxobacter dehalogenans to uncover novel genetic elements.
Methodology:
Performs detailed frame analysis that quantitatively assesses GC usage variations across codon frames, provides statistical characterization of three-base compositional periodicities, and generates graphical outputs for visual inspection.
Topics
Details
- Tool Type:
- command-line tool
- Operating Systems:
- Linux, Windows, Mac
- Added:
- 8/3/2017
- Last Updated:
- 11/25/2024
Operations
Publications
Oden S, Brocchieri L. Quantitative frame analysis and the annotation of GC-rich (and other) prokaryotic genomes. An application to <i>Anaeromyxobacter dehalogenans</i>. Bioinformatics. 2015;31(20):3254-3261. doi:10.1093/bioinformatics/btv339. PMID:26048600. PMCID:PMC4595893.