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.

Documentation

Links