Search results
Results from the WOW.Com Content Network
Then, p 2 is the fraction of the population homozygous for the first allele, 2pq is the fraction of heterozygotes, and q 2 is the fraction homozygous for the alternative allele. If the first allele is dominant to the second then the fraction of the population that will show the dominant phenotype is p 2 + 2 pq , and the fraction with the ...
Allele frequency, or gene frequency, is the relative frequency of an allele (variant of a gene) at a particular locus in a population, expressed as a fraction or percentage. [1]
Gene flow is the transfer of alleles from one population to another population through immigration of individuals. In population genetics, gene flow (also known as migration and allele flow) is the transfer of genetic material from one population to another. If the rate of gene flow is high enough, then two populations will have equivalent ...
In the simplest case of a single locus with two alleles denoted A and a with frequencies f(A) = p and f(a) = q, respectively, the expected genotype frequencies under random mating are f(AA) = p 2 for the AA homozygotes, f(aa) = q 2 for the aa homozygotes, and f(Aa) = 2pq for the heterozygotes.
Each autosomal gene is therefore represented by two copies, or alleles, with one copy inherited from each parent at fertilization. The expressed allele is dependent upon its parental origin. For example, the gene encoding insulin-like growth factor 2 (IGF2/Igf2) is only expressed from the allele inherited from the male. Although imprinting ...
A microsatellite is a tract of tandemly repeated (i.e. adjacent) DNA motifs that range in length from one to six or up to ten nucleotides (the exact definition and delineation to the longer minisatellites varies from author to author), [1] [6] and are typically repeated 5–50 times.
Autosomal dominant-recessive inheritance is made possible by the fact that the individuals of most species (including all higher animals and plants) have two alleles of most hereditary predispositions because the chromosomes in the cell nucleus are usually present in pairs . Carriers can be female or male as the autosomes are homologous ...
DNA molecule 1 differs from DNA molecule 2 at a single base-pair location (a C/A polymorphism). A haplotype (haploid genotype) is a group of alleles in an organism that are inherited together from a single parent. [1] [2] Many organisms contain genetic material which is inherited from two parents.