First-degree relationships and genotyping errors deciphered by a high-density SNP array in a Duroc×Iberian pig

L Gomez-Raya1, E Gómez Izquierdo2, E de Mercado de la Peña3

  • 1Departamento de Mejora Genética Animal, Instituto Nacional de Investigación y Tecnología Agraria y Alimentaria (INIA-CSIC), Ctra. de La Coruña km 7.5, 28040, Madrid, Spain. luis.gomez.raya@csic.es.

BMC Genomic Data
|February 18, 2022
PubMed
Summary

Genetic exclusion principles accurately verify animal relationships and estimate genotyping errors in genomic selection studies. This method confirms parentage and identifies problematic SNPs, enhancing data reliability.

Related Concept Videos

Single Nucleotide Polymorphisms-SNPs01:05

Single Nucleotide Polymorphisms-SNPs

A single nucleotide polymorphism or SNP is a single nucleotide variation at a specific genomic position in a large population. It is the most prevalent type of sequence variation found in the human genome. Point mutations that occur in more than 1% of the population qualify as SNPs. These are present once every 1000 nucleotides on an average in the human genome. Replacement of a purine with another purine (A/G) or a pyrimidine with another pyrimidine (C/T) is known as a transition. In contrast,...
16.5K
Monohybrid Crosses01:20

Monohybrid Crosses

Overview
232.4K
Incomplete Dominance01:43

Incomplete Dominance

Gregor Mendel's work (1822 - 1884) was primarily focused on pea plants. Through his initial experiments, he determined that every gene in a diploid cell has two variants called alleles inherited from each parent. He suggested that amongst these two alleles, one allele is dominant in character and the other recessive. The combination of alleles determines the phenotype of a gene in an organism.
26.1K
Pedigree Analysis01:35

Pedigree Analysis

Overview
85.8K
Comparing Copy Number Variations and SNPs02:26

Comparing Copy Number Variations and SNPs

Sequencing of the human genome has opened up several best-kept secrets of the genome. Scientists have identified thousands of genome variations that exist within a population. These variations can be a single nucleotide or a larger chromosomal variation.
Copy number variations or CNVs are the structural variations that cover more than 1kb of DNA sequence. The single nucleotide polymorphism (SNP), on the other hand, is a single nucleotide change or a point mutation that is found in more than 1%...
18.0K