IndelsRNAmute
IndelsRNAmute predicts the effects of insertion, deletion, and substitution mutations on RNA secondary structure to identify deleterious mutations affecting structural RNAs.
Key Features:
- Extension of RNAmute and MultiRNAmute: Extends RNAmute and MultiRNAmute by adding prediction of insertion and deletion (indel) mutations alongside substitutions.
- Suboptimal folding–based algorithm: Uses suboptimal folding solutions to efficiently predict multiple deleterious mutations, including combinations of deletions, insertions, and substitutions.
- User-defined mutation sets: Supports specification of the number and types of mutations to investigate, enabling modeling of combinatorial mutation scenarios.
- Computational complexity handling: Addresses the computational challenges of finding the most deleterious mutation sets in structural RNAs and provides a more practical alternative to brute-force enumeration for long sequences.
Scientific Applications:
- Site-directed mutagenesis: Identifies indel and substitution targets that are likely to disrupt critical RNA secondary-structure motifs for experimental validation.
- Viral research: Evaluates how specific indels and substitutions may disrupt essential structural elements in RNA viruses and affect viral functionality.
- Functional genomics: Predicts impacts of diverse mutation types on RNA stability and structure to support studies of genetic regulation and RNA function.
Methodology:
Builds on the MultiRNAmute method and incorporates strategies for predicting insertion and deletion mutations by stabilizing suboptimal folding solutions or destabilizing the wild-type optimal fold to predict deleterious effects, providing greater efficiency than brute-force approaches.
Topics
Details
- Cost:
- Free of charge
- Tool Type:
- command-line tool
- Operating Systems:
- Windows
- Added:
- 12/29/2022
- Last Updated:
- 11/24/2024
Operations
Data Inputs & Outputs
Fold recognition
Inputs
Outputs
Publications
Churkin A, Ponty Y, Barash D. IndelsRNAmute: predicting deleterious multiple point substitutions and indels mutations. BMC Bioinformatics. 2022;23(S8). doi:10.1186/s12859-022-04943-0. PMID:36241988. PMCID:PMC9569039.