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A little mathematics of the multiplication-table type is enough to show that in the next generation the numbers will be as (p + q) 2:2(p + q)(q + r):(q + r) 2, or as p 1:2q 1:r 1, say. The interesting question is: in what circumstances will this distribution be the same as that in the generation before?
"Mono-" means "one"; this cross indicates that the examination of a single trait. This could mean (for example) eye color. Each genetic locus is always represented by two letters. So in the case of eye color, say "B = Brown eyes" and "b = green eyes". In this example, both parents have the genotype Bb. For the example of eye color, this would ...
V P = V E + V G, where the terms refer to variation in phenotype, environment, and genotype respectively. [1] Broad sense heritability (H 2, or H B) refers to the phenotypic differences arising from all genetic effects, and can be described as the ratio of genotypic variation to that of phenotypic variation in the population, or: H 2 = V G / V P.
Population genetics describes the genetic composition of a population, including allele frequencies, and how allele frequencies are expected to change over time. The Hardy–Weinberg law describes the expected equilibrium genotype frequencies in a diploid population after random mating. Random mating alone does not change allele frequencies ...
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 ...
A genetic marker is a gene or DNA sequence with a known location on a chromosome that can be used to identify individuals or species. It can be described as a variation (which may arise due to mutation or alteration in the genomic loci) that can be observed.
Genotype can also be used to refer to the alleles or variants an individual carries in a particular gene or genetic location. [2] The number of alleles an individual can have in a specific gene depends on the number of copies of each chromosome found in that species, also referred to as ploidy .
Polymorphisms can be identified in the laboratory using a variety of methods. Many methods employ PCR to amplify the sequence of a gene. Once amplified, polymorphisms and mutations in the sequence can be detected by DNA sequencing, either directly or after screening for variation with a method such as single strand conformation polymorphism analysis.