SeLOX
SeLOX identifies degenerate lox-like sites in genomic sequences to support site-specific recombinase-based genome engineering such as Cre recombinase-mediated excision of integrated retroviruses.
Key Features:
- Degenerate lox-like site detection: Searches for two inverted repeats flanking a variable-length spacer characteristic of lox-like recombination sites.
- Position weight matrix scoring: Calculates a position weight matrix based on known lox-like sequences to score candidate sites.
- Binary sequence transformation: Converts sequences into binary space to enable efficient encoding of nucleotide patterns.
- Bit-wise Boolean comparisons: Uses bit-wise AND operations on binary-encoded sequences for rapid and accurate matching.
- Large-scale genome searches: Applies the search approach to large genomic datasets, including whole-genome scans.
Scientific Applications:
- Cre-mediated retrovirus excision (HIV-1 LTR): Identification of lox-like sites suitable for Cre recombinase excision of integrated HIV-1 proviral long terminal repeats (LTRs).
- Yeast recombinase target discovery: Detection of lox-like sites compatible with six different yeast recombinases.
- Human genome screening: Genome-wide search for Cre-type recombination sites across the human genome.
- Site-specific recombination engineering: Supports selection of target sites for site-specific recombinase applications in genome engineering experiments.
Methodology:
SeLOX computes a position weight matrix from known lox-like sequences, converts target sequences into binary representations, and employs bit-wise AND Boolean comparisons to locate inverted repeats flanking variable-length spacers.
Topics
Details
- Tool Type:
- web application
- Added:
- 3/25/2017
- Last Updated:
- 11/25/2024
Operations
Publications
Surendranath V, Chusainow J, Hauber J, Buchholz F, Habermann BH. SeLOX—a locus of recombination site search tool for the detection and directed evolution of site-specific recombination systems. Nucleic Acids Research. 2010;38(suppl_2):W293-W298. doi:10.1093/nar/gkq523. PMID:20529878.