Mendel

Mendel performs likelihood-based statistical analysis for gene mapping and association studies, supporting linkage and genome-wide association analyses across pedigree and population genetic data.


Key Features:

  • Likelihood-based inference: Implements likelihood-based statistical analysis for genetic data.
  • Gene mapping methods: Provides a suite of gene mapping methods including parametric linkage analyses in large pedigrees.
  • Genome-wide association: Supports genome-wide association studies (GWAS) including analysis of rare variants.
  • Trait support: Analyzes both qualitative and quantitative traits.
  • Sample types: Processes pedigree and population samples.
  • Marker density: Handles datasets with limited loci as well as dense single nucleotide polymorphism (SNP) data.
  • Statistical tests: Implements a comprehensive range of statistical genetic tests, encompassing common methodologies and several novel approaches.

Scientific Applications:

  • Parametric linkage mapping: Mapping Mendelian loci in large pedigrees using parametric linkage analysis.
  • GWAS and rare-variant association: Identifying associations in genome-wide association studies including rare variant analysis.
  • Trait genetics: Dissecting genetic architecture of qualitative and quantitative traits.
  • Pedigree and population analysis: Analysis of genetic variation and inheritance in both pedigree and population samples.
  • Sparse and dense marker studies: Mapping and association analyses using limited loci datasets and dense SNP arrays.

Methodology:

Uses likelihood-based statistical analysis, parametric linkage analysis, and genome-wide association methods including rare-variant tests.

Topics

Collections

Details

License:
Other
Tool Type:
command-line tool, desktop application
Operating Systems:
Linux, Windows, Mac
Added:
8/20/2017
Last Updated:
11/25/2024

Operations

Publications

Lange K, Papp JC, Sinsheimer JS, Sripracha R, Zhou H, Sobel EM. Mendel: the Swiss army knife of genetic analysis programs. Bioinformatics. 2013;29(12):1568-1570. doi:10.1093/bioinformatics/btt187. PMID:23610370. PMCID:PMC3673222.

Documentation