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

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.