MSQT

MSQT extracts SNPs from multiple sequence alignments and stores them to support SNP genotyping assay design and genetic mapping and association studies.


Key Features:

  • Data Extraction and Storage: Processes multiple sequence alignment data to identify SNPs and stores them in a structured database.
  • Output Formats for Assay Design: Exports SNP data in formats directly applicable to designing SNP genotyping assays.

Scientific Applications:

  • Genotyping and Association Mapping: Identifies informative markers between groups of individuals to support genotyping and association mapping projects.
  • Development of Genotyping Assays: Applied to Arabidopsis thaliana sequence data to facilitate development of SNP genotyping assays distinguishing Col-0 from five other strains.
  • Genetic Mapping Among Wild Strains: Selects SNPs with intermediate allele frequencies and develops them into markers for genetic mapping among random pairs of wild strains.

Methodology:

MSQT analyzes multiple sequence alignment data to pinpoint SNPs, catalogs them in a database, and exports the results in formats for genotyping assay design.

Topics

Details

Tool Type:
command-line tool
Operating Systems:
Linux, Mac
Programming Languages:
Perl
Added:
12/18/2017
Last Updated:
11/25/2024

Operations

Publications

Warthmann N, Fitz J, Weigel D. MSQT for choosing SNP assays from multiple DNA alignments. Bioinformatics. 2007;23(20):2784-2787. doi:10.1093/bioinformatics/btm428. PMID:17785349.

Documentation

Links