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The Punnett square is a square diagram that is used to predict the genotypes of a particular cross or breeding experiment. It is named after Reginald C. Punnett, who devised the approach in 1905. [3][4][5][6][7][8] The diagram is used by biologists to determine the probability of an offspring having a particular genotype.
Punnett square for three-allele case (left) and four-allele case (right). White areas are homozygotes. Colored areas are heterozygotes. Consider an extra allele frequency, r. The two-allele case is the binomial expansion of (p + q) 2, and thus the three-allele case is the trinomial expansion of (p + q + r) 2.
Mendelian inheritance (also known as Mendelism) is a type of biological inheritance following the principles originally proposed by Gregor Mendel in 1865 and 1866, re-discovered in 1900 by Hugo de Vries and Carl Correns, and later popularized by William Bateson. [1]
Genotype frequency in a population is the number of individuals with a given genotype divided by the total number of individuals in the population. [2] In population genetics, the genotype frequency is the frequency or proportion (i.e., 0 < f < 1) of genotypes in a population. Although allele and genotype frequencies are related, it is ...
Punnett square of the possible genotypes and phenotypes of children given genotypes and phenotypes of their mother (rows) and father (columns) shaded by phenotype. Blood groups are inherited from both parents. The ABO blood type is controlled by a single gene (the ABO gene) with three types of alleles inferred from classical genetics: i, I A ...
Genetic linkage is the tendency of DNA sequences that are close together on a chromosome to be inherited together during the meiosis phase of sexual reproduction.Two genetic markers that are physically near to each other are unlikely to be separated onto different chromatids during chromosomal crossover, and are therefore said to be more linked than markers that are far apart.
Punnett square: If the other parent does not have the recessive genetic disposition, it does not appear in the phenotype of the children, but on the average 50% of them become carriers. A hereditary carrier ( genetic carrier or just carrier ), is a person or other organism that has inherited a recessive allele for a genetic trait or mutation ...
In genetics, the phenotype (from Ancient Greek φαίνω (phaínō) 'to appear, show' and τύπος (túpos) 'mark, type') is the set of observable characteristics or traits of an organism. [1][2] The term covers the organism's morphology (physical form and structure), its developmental processes, its biochemical and physiological properties ...