MCPtaggR

MCPtaggR improves genotype calling accuracy in reduced representation sequencing (RRS) data by identifying and filtering mismapping- and bias-prone markers using collinearity information between parental genomes within the mappable collinear polymorphic tag genotyping (MCPtagg) pipeline.


Key Features:

  • Elimination of error-prone markers: Filters markers that produce mismapping or biased mapping when RRS reads with mismatches are mapped onto a reference genome.
  • Collinearity-based filtering: Leverages marker collinearity information derived from genome sequence comparisons of parent organisms in biparental cross populations to identify and exclude problematic markers prior to genotype calling.
  • Sequencing technology compatibility: Designed for reduced representation sequencing approaches including genotyping-by-sequencing (GBS).
  • Assembly compatibility: Demonstrated performance with polished genome assemblies and does not require de novo assembly for accurate genotype calling.
  • Implementation: Distributed as an R package that implements the MCPtagg pipeline for marker filtering and genotype calling workflows.
  • Evaluation on empirical data: Validated using real GBS data from a rice F2 population to assess genotyping accuracy.

Scientific Applications:

  • Plant and animal breeding: Improves genotype accuracy for mapping traits and informing genetic selection in breeding programs.
  • Population genetics: Reduces genotyping errors in studies of allele frequencies, linkage, and population structure using RRS data.
  • Evolutionary biology: Enhances reliability of genotype data for analyses of genetic diversity and evolutionary inference.

Methodology:

Maps RRS reads to a reference genome, filters markers with mismapping- or bias-associated signals, uses marker collinearity from parental genome sequence comparisons in biparental crosses to exclude error-prone markers prior to genotype calling, and was evaluated on GBS data from a rice F2 population and on polished genome assemblies without de novo assembly.

Topics

Details

License:
GPL-3.0
Cost:
Free of charge
Tool Type:
library
Operating Systems:
Mac, Linux, Windows
Programming Languages:
R
Added:
4/19/2024
Last Updated:
11/24/2024

Operations

Publications

Furuta T, Yamamoto T. MCPtaggR: R package for accurate genotype calling in reduced representation sequencing data by eliminating error-prone markers based on genome comparison. DNA Research. 2023;31(1). doi:10.1093/dnares/dsad027. PMID:38134958. PMCID:PMC10799318.

PMID: 38134958
Funding: - Japan Society for the Promotion of Science: JP20K15503, JP23H02185

Documentation