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Related Concept Videos

Genomics02:02

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...
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.
Genomic DNA in Eukaryotes00:58

Genomic DNA in Eukaryotes

Eukaryotes have large genomes compared to prokaryotes. To fit their genomes into a cell, eukaryotic DNA is packaged extraordinarily tightly inside the nucleus. To achieve this, DNA is tightly wound around proteins called histones, which are packaged into nucleosomes that are joined by linker DNA and coil into chromatin fibers. Additional fibrous proteins further compact the chromatin, which is recognizable as chromosomes during certain phases of cell division.
Human Genetics01:28

Human Genetics

Human genetics provides a profound framework for understanding the interplay between genetic predispositions and human psychology. At the heart of this discipline lies the study of how genes influence physical traits, behaviors, and susceptibility to diseases. Each person carries a unique genetic code that subtly or significantly shapes their psychological and behavioral landscape.
The complex relationship between genetics and psychology is observable through common biological components such...
Animal Mitochondrial Genetics02:59

Animal Mitochondrial Genetics

Among all the organelles in an animal cell, only mitochondria have their own independent genomes. Animal mitochondrial DNA is a double-stranded, closed-circular molecule with around 20,000 base pairs. Mitochondrial DNA is unique in that one of its two strands, the heavy, or H, -strand is guanine rich, whereas the complementary strand is cytosine rich and called the light, or L, -strand. Compared to nuclear DNA, mitochondrial DNA has a very low percentage of non-coding regions and is marked by...
From DNA to Protein03:06

From DNA to Protein

The flow of genetic information in cells from DNA to mRNA to protein is described by the central dogma, which states that genes specify the sequence of mRNAs, which in turn specify the sequence of amino acids making up all proteins. The decoding of one molecule to another is performed by specific proteins and RNAs. Because the information stored in DNA is so central to cellular function, it makes intuitive sense that the cell would make mRNA copies of this information for protein synthesis...

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Related Experiment Video

Updated: Jul 2, 2026

Analysis of Chromosome Segregation, Histone Acetylation, and Spindle Morphology in Horse Oocytes
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Analysis of Chromosome Segregation, Histone Acetylation, and Spindle Morphology in Horse Oocytes

Published on: May 11, 2017

The horse genome.

B P Chowdhary1, T Raudsepp

  • 1Department of Veterinary Integrative Biosciences, College of Veterinary Medicine and Biomedical Sciences, Texas A&M University, College Station, Tex., USA.

Genome Dynamics
|August 30, 2008
PubMed
Summary

The horse genome map is now the densest among domestic animals, aiding research into equine health, traits, and performance. Further genomic tools position the horse as an ideal candidate for whole genome sequencing.

Area of Science:

  • Equine Genomics
  • Comparative Genomics
  • Animal Genetics

Background:

  • Horse genome analysis has advanced significantly in the last decade.
  • Multiple mapping techniques have been employed to create comprehensive equine genome maps.

Purpose of the Study:

  • To detail the current state of equine genome mapping and its applications.
  • To highlight the horse's readiness for whole genome sequencing.

Main Methods:

  • Generation of synteny, genetic linkage, radiation hybrid, cytogenetic, and comparative maps.
  • Development of a high-resolution equine gene map with approximately 4,000 markers.
  • Creation of a physical map using bacterial artificial chromosome (BAC) clones and end-sequencing.

Main Results:

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Navigating MARRVEL, a Web-Based Tool that Integrates Human Genomics and Model Organism Genetics Information
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Navigating MARRVEL, a Web-Based Tool that Integrates Human Genomics and Model Organism Genetics Information

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  • The equine gene map is the densest among non-sequenced domestic animals, with a resolution of approximately 700 kb.
  • The map facilitates research into genes affecting horse health, disease resistance, reproduction, and athletic performance.
  • A physical map of ~150,000 BAC clones is under development.

Conclusions:

  • The comprehensive genomic resources make the horse an excellent candidate for whole genome sequencing.
  • Functional studies and expression-based analyses are emerging areas in equine genomics.
  • Industry support is crucial for the advancement of equine genome sequencing projects.