CBCAnalyzer 1.1 beta
CBCAnalyzer 1.1 beta analyzes compensatory base changes (CBCs) in RNA sequences to support studies of molecular evolution, species differentiation, and RNA structure–function relationships.
Key Features:
- CTTransform module: Reads ct, RNAviz ct, and Mac ct file formats and converts RNA secondary-structure representations into a bracket-dot-bracket format.
- CBCDetect module: Counts compensatory base changes (CBCs) across all aligned sequence pairs and produces a count matrix of CBC occurrences.
- CBCTree module: Reconstructs a phylogram from the CBC count matrix using the BIONJ (Biased-Neighbor-Joining) algorithm.
- Interoperability: Generates bracket-dot-bracket output compatible with RNAforester, RNAmovie, and MARNA.
- Implementation: Implemented in C++ for computational processing.
Scientific Applications:
- Molecular evolution: Analysis of CBCs to investigate nucleotide co-variation and evolutionary change in RNA populations.
- Species differentiation: Use of CBC counts to inform species delimitation and differentiation assessments.
- Detection of sexual incompatibility: Identification of CBC patterns that have been associated with species exhibiting sexual incompatibility.
- RNA structure–function studies: Integration of secondary-structure representations with sequence comparisons to study structure–function relationships.
- Phylogenetic inference: Reconstruction and visualization of evolutionary relationships based on CBC-derived distance information.
Methodology:
CTTransform reads ct / RNAviz ct / Mac ct files and outputs bracket-dot-bracket format; CBCDetect counts CBCs across aligned sequence pairs and generates a CBC count matrix; CBCTree builds a phylogram from that count matrix using the BIONJ algorithm.
Topics
Details
- Tool Type:
- desktop application
- Operating Systems:
- Linux, Windows, Mac
- Programming Languages:
- C++
- Added:
- 12/18/2017
- Last Updated:
- 12/10/2018
Operations
Publications
Wolf M, et al. CBCAnalyzer: inferring phylogenies based on compensatory base changes in RNA secondary structures. In Silico Biol. 2005; 5:291-4.
PMID: 15996120