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Ohio State creates first equine gene chip
Ohio State creates first equine gene chip

... Researchers at Ohio State have created the first DNA gene chip that contains thousands of genes for a horse and one of the first gene chips for a domestic animal. The new chip houses more than 3,200 expressed horse genes on a sliver of glass about the size of a postage stamp. When researchers began ...
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... Syvånen, Uppsala University, Sweden, and Andres Metspalu, Tartu University, Estonia), or via a ligase assay (Ed Southern, Oxford University, UK) were shown to distinguish SNPs in heterozygote and homozygote form more accurately than hybridisation-based methods. Nonetheless, hybridisation to high de ...
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(GWAS) and Personalized Medicine

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... All societies in this study have had contact with other societies, making it hard to discern if there is an effect of auto-correlation or not. This is particularly true of American Indians who are known to share common ancestry with each other. • Researchers corrected for this by including all avail ...
PPT Version - OMICS International
PPT Version - OMICS International

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When completed, this form will contain Protected Health Information
When completed, this form will contain Protected Health Information

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... (http://evs.gs.washington.edu/EVS/). For whole genome sequencing, we used 54 individual genomes sequenced by Complete Genomics (www.completegenomics.com). For both methods, we observed a very low sequencing coverage of SHANK1 and SHANK3 (Figure S3). Whole genome sequencing seems to be a better appro ...
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... product of the probability of the events occurring separately. 2. Chance of inheriting a specific allele from one parent and a specific allele from another is 1/2 x 1/2 or 1/4. 3. Possible combinations for the alleles Hh x Hh are the following: ...
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The Gene - Genetics
The Gene - Genetics

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No Slide Title
No Slide Title

... From Genes to Behaviour.  Epigenesis describes the study of the ways in which genes bring about their effects on growth and development.  Badcock (2000): it is wrong to think of genes as forming a 'blueprint' for the body and mind as genes do not specify every detail of an individual.  Genes ini ...
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Chapter 3 Outline

... III. Nature and Nurture: Influences of Heredity and Environment A. Studying the Relative Influences of Heredity and Environment  Behavioral genetics: Quantitative study of how much heredity and environment influence particular traits. 1. Measuring Heritability  Heritability: Statistical estimate ...
Genetics Slides
Genetics Slides

... Most human traits are polygenic, which means they are controlled by multiple genes. –  This leads to a wide array of phenotypes. –  Simple Punnett squares do NOT work for polygenic traits. §  EX: Human height & eye color. ...
Signatures of Selection in the Human Olfactory Receptor OR5I1 Gene
Signatures of Selection in the Human Olfactory Receptor OR5I1 Gene

... primates. Nonetheless, this olfactory decline opens an opportunity for evolutionary innovation and improvement. In the present study, we focus on an OR gene, OR5I1, which had previously been shown to present an excess of amino acid replacement substitutions between humans and chimpanzees. We analyze ...
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Human genetic variation



Human genetic variation is the genetic differences both within and among populations. There may be multiple variants of any given gene in the human population (genes), leading to polymorphism. Many genes are not polymorphic, meaning that only a single allele is present in the population: the gene is then said to be fixed. On average, in terms of DNA sequence all humans are 99.9% similar to any other humans.No two humans are genetically identical. Even monozygotic twins, who develop from one zygote, have infrequent genetic differences due to mutations occurring during development and gene copy-number variation. Differences between individuals, even closely related individuals, are the key to techniques such as genetic fingerprinting. Alleles occur at different frequencies in different human populations, with populations that are more geographically and ancestrally remote tending to differ more.Causes of differences between individuals include the exchange of genes during meiosis and various mutational events. There are at least two reasons why genetic variation exists between populations. Natural selection may confer an adaptive advantage to individuals in a specific environment if an allele provides a competitive advantage. Alleles under selection are likely to occur only in those geographic regions where they confer an advantage. The second main cause of genetic variation is due to the high degree of neutrality of most mutations. Most mutations do not appear to have any selective effect one way or the other on the organism. The main cause is genetic drift, this is the effect of random changes in the gene pool. In humans, founder effect and past small population size (increasing the likelihood of genetic drift) may have had an important influence in neutral differences between populations. The theory that humans recently migrated out of Africa supports this.The study of human genetic variation has both evolutionary significance and medical applications. It can help scientists understand ancient human population migrations as well as how different human groups are biologically related to one another. For medicine, study of human genetic variation may be important because some disease-causing alleles occur more often in people from specific geographic regions. New findings show that each human has on average 60 new mutations compared to their parents.Apart from mutations, many genes that may have aided humans in ancient times plague humans today. For example, it is suspected that genes that allow humans to more efficiently process food are those that make people susceptible to obesity and diabetes today.
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