SeqFIRE
SeqFIRE extracts sequence features and indel regions from multiple protein sequence alignments to identify conserved blocks, indels (insertions and deletions), and fast-evolving sites for phylogenomic analyses.
Key Features:
- Automated Indel Extraction: Identifies and extracts indels (insertions and deletions) from protein sequence alignments as phylogenetic markers.
- Conserved Block Identification: Extracts blocks of conserved alignment columns to delineate stable regions across sequences.
- Fast-Evolving Site Detection: Detects fast-evolving sites using a combination of conservation metrics and entropy calculations.
- Parameter Customization: Allows adjustment of major variables for indel detection, conserved block extraction, and site-rate identification.
- Comprehensive Output Options: Produces numbered indel lists, alignments in NEXUS format with options for annotated or removed indels, and matrices containing only indel information.
Scientific Applications:
- Phylogenomics: Enables analysis of large multigene datasets to incorporate indel and conserved-block information into phylogenetic inference.
- Phylogenetic Marker Discovery and Molecular Evolution: Facilitates identification of novel phylogenetic markers and assessment of molecular evolutionary patterns using indels and fast-evolving sites.
Methodology:
Analyzes multiple sequence alignments to extract conserved and variable regions and uses algorithms that combine conservation metrics and entropy calculations to identify indels and fast-evolving sites; outputs include numbered indel lists, NEXUS-formatted alignments with annotated or removed indels, and indel-only matrices.
Topics
Details
- Tool Type:
- web application
- Operating Systems:
- Linux, Windows, Mac
- Programming Languages:
- PHP, Python
- Added:
- 3/25/2017
- Last Updated:
- 11/25/2024
Operations
Publications
Ajawatanawong P, Atkinson GC, Watson-Haigh NS, MacKenzie B, Baldauf SL. SeqFIRE: a web application for automated extraction of indel regions and conserved blocks from protein multiple sequence alignments. Nucleic Acids Research. 2012;40(W1):W340-W347. doi:10.1093/nar/gks561. PMID:22693213. PMCID:PMC3394284.