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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,...
Genome-wide Association Studies-GWAS01:11

Genome-wide Association Studies-GWAS

Genome-wide association studies or GWAS are used to identify whether common SNPs are associated with certain diseases. Suppose specific SNPs are more frequently observed in individuals with a particular disease than those without the disease. In that case, those SNPs are said to be associated with the disease. Chi-square analysis is performed to check the probability of the allele likely to be associated with the disease.
GWAS does not require the identification of the target gene involved in...
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%...
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Modern Molecular Taxonomy

Advancements in molecular biology have revolutionized the identification and characterization of bacteria, with multiple methods leveraging DNA sequencing for enhanced precision. As sequencing technologies improve and costs decline, these approaches are increasingly used in clinical, environmental, and evolutionary studies.Multilocus Sequence Typing (MLST) examines several housekeeping genes, essential chromosomal genes encoding cellular functions, to distinguish strains. Approximately...
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Genomics

Genomics is the science of genomes: it is the study of all the genetic material of an organism. In humans, the genome consists of information carried in 23 pairs of chromosomes in the nucleus, as well as mitochondrial DNA. In genomics, both coding and non-coding DNA is sequenced and analyzed. Genomics allows a better understanding of all living things, their evolution, and their diversity. It has a myriad of uses: for example, to build phylogenetic trees, to improve productivity and...
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Multi-species Conserved Sequences

Next-generation sequencing technologies have created large genomic databases of a variety of animals and plants. Ever since the human genome project was completed, scientists studied the genome of primates, mammals, and other phylogenetically distant living beings. Such large-scaleĀ  studies have provided new insights into the evolutionary relationship between organisms.
Although the genome of each species varies greatly from each other, a few sequences are highly conserved. Such conserved DNA...

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Candidate Gene Testing in Clinical Cohort Studies with Multiplexed Genotyping and Mass Spectrometry
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Brief introduction to whole-genome selection in cattle using single nucleotide polymorphisms.

G E Seidel1

  • 1Animal Reproduction and Biotechnology Laboratory, Colorado State University, Fort Collins, CO 80523-1683, USA. gseidel@colostate.edu

Reproduction, Fertility, and Development
|December 17, 2009
PubMed
Summary

Genomic selection using single nucleotide polymorphisms (SNPs) can nearly double genetic gain in dairy cattle. This powerful tool requires accurate phenotypes and population-specific analyses for optimal genetic improvement.

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Area of Science:

  • Animal Genetics
  • Genomic Selection
  • Quantitative Genetics

Background:

  • Genomic selection utilizing single nucleotide polymorphisms (SNPs) represents an advancement in genetic improvement strategies.
  • SNP profiles are generated using diagnostic chips, enabling genome-wide analysis.

Purpose of the Study:

  • To evaluate the efficacy of genomic selection using SNPs in cattle breeding.
  • To determine the impact of SNP information on the rate of genetic improvement for various traits.

Main Methods:

  • Matching animal phenotypes with their respective SNP profiles through mathematical analysis.
  • Developing population-specific SNP analysis systems for different cattle breeds.

Main Results:

  • Genomic selection can nearly double the rate of genetic improvement in dairy cattle compared to traditional methods.
  • The accuracy and value of SNP systems are highly dependent on the number of accurate phenotypes available.
  • Increasing the number of evaluated bulls significantly enhances genetic gain.

Conclusions:

  • Genomic selection with SNPs offers substantial potential for accelerating genetic gain in cattle.
  • Accurate, population-specific SNP evaluation systems and sufficient phenotypic data are crucial for successful implementation.
  • Evaluating embryos via SNP analysis can minimize generation intervals and maximize the technology's value.