LOT
LOT performs linkage analysis of ordinal traits in pedigree datasets to model inheritance patterns and test for linkage between genetic markers and ordinal phenotypes.
Key Features:
- Latent-variable proportional-odds logistic model: Models ordinal trait outcomes using a latent-variable extension of the proportional-odds logistic framework.
- Likelihood-ratio test for linkage: Evaluates evidence of linkage between genetic markers and ordinal traits using likelihood-ratio testing.
- Pedigree-based analysis: Operates on pedigree datasets to relate familial structure to trait distributions.
- Ordinal-trait focus: Specifically targets traits measured on ordinal scales rather than binary or continuous measures.
- Inheritance-pattern modeling: Relates latent genetic effects to the distribution of ordinal traits within families to capture underlying genetic architecture.
Scientific Applications:
- Linkage analysis of ordinal phenotypes: Detects linkage signals for phenotypes recorded on ordered categorical scales within family data.
- Behavioral disorder genetics: Supports genetic investigations of behavioral disorders that are rated on ordinal scales.
- Complex disease studies: Facilitates analysis of complex human conditions where traits are not easily quantifiable but exhibit ordered categories.
- Family-based genetic research: Enables studies of transmission of ordinal traits across generations in pedigree-based designs.
Methodology:
Implements a latent-variable proportional-odds logistic model to relate latent genetic effects to the distribution of ordinal traits within families and applies likelihood-ratio tests to assess linkage between genetic markers and ordinal traits.
Topics
Details
- Tool Type:
- desktop application
- Operating Systems:
- Linux, Windows, Mac
- Programming Languages:
- Java
- Added:
- 12/18/2017
- Last Updated:
- 11/25/2024
Operations
Publications
Zhang M, Feng R, Chen X, Hu B, Zhang H. LOT: a tool for linkage analysis of ordinal traits for pedigree data. Bioinformatics. 2008;24(15):1737-1739. doi:10.1093/bioinformatics/btn258. PMID:18535081. PMCID:PMC2566542.