Search results
Results from the WOW.Com Content Network
Human genetics is the study of inheritance as it occurs in human beings. Human genetics encompasses a variety of overlapping fields including: classical genetics , cytogenetics , molecular genetics , biochemical genetics , genomics , population genetics , developmental genetics , clinical genetics , and genetic counseling .
In genetics, a centimorgan (abbreviated cM) or map unit (m.u.) is a unit for measuring genetic linkage. It is defined as the distance between chromosome positions (also termed loci or markers) for which the expected average number of intervening chromosomal crossovers in a single generation is 0.01. It is often used to infer distance along a ...
Coalescent theory, a retrospective model of population genetics; Crown group; Genealogy, the study of families and the tracing of their lineages and history; Genetic distance, the genetic divergence between species or between populations within a species; Lowest common ancestor, an analogous concept in graph theory and computer science
The identical ancestors point for Homo sapiens has been the subject of debate. In 2003 Rohde estimated it to be between 5000 and 15,000 years ago. [2] In 2004, Rohde, Olson and Chang showed through simulations that, given the false assumption of random mate choice without geographic barriers, the Identical Ancestors Point for all humans would be surprisingly recent, on the order of 5,000 ...
Example calculation of a paternity index. In paternity testing, Paternity Index (PI) is a calculated value generated for a single genetic marker or locus (chromosomal location or site of DNA sequence of interest) and is associated with the statistical strength or weight of that locus in favor of or against parentage given the phenotypes of the tested participants and the inheritance scenario.
Recently reported estimates of the human genome-wide mutation rate. The human germline mutation rate is approximately 0.5×10 −9 per basepair per year. [1]In genetics, the mutation rate is the frequency of new mutations in a single gene, nucleotide sequence, or organism over time. [2]
Two fundamental calculations are central to population genetics: allele frequencies and genotype frequencies. [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 ]
For example, the step-wise reintroduction strategy of the Alpine Ibex in the Swiss Alps created several strong population bottlenecks that reduced the genetic diversity of the newly introduced individuals. The effect of inbreeding in the resulting sub-populations could be studied by measuring the runs of homozygosity in different individuals.