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Analysis of the pedigree using the principles of Mendelian inheritance can determine whether a trait has a dominant or recessive pattern of inheritance. Pedigrees are often constructed after a family member afflicted with a genetic disorder has been identified. This individual, known as the proband, is indicated on the pedigree by an arrow. [5]
Mendelian traits behave according to the model of monogenic or simple gene inheritance in which one gene corresponds to one trait. Discrete traits (as opposed to continuously varying traits such as height) with simple Mendelian inheritance patterns are relatively rare in nature, and many of the clearest examples in humans cause disorders.
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In this pedigree chart, G is the progeny of C and F, and C is the biological uncle of F. To find the coefficient of inbreeding of G, first locate a loop that leads from G to the common ancestor through one parent and back down to the other parent without going through the same individual twice.
A DNA segment is identical by state (IBS) in two or more individuals if they have identical nucleotide sequences in this segment. An IBS segment is identical by descent (IBD) in two or more individuals if they have inherited it from a common ancestor without recombination, that is, the segment has the same ancestral origin in these individuals.
The advantages of population based association mapping, utilizing a sample of individuals from the germplasm collections or a natural population, over traditional QTL-mapping in biparental crosses, primarily are due to availability of broader genetic variations with wider background for marker and trait correlations.
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