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  2. Genetic variation - Wikipedia

    en.wikipedia.org/wiki/Genetic_variation

    Genetic variation can be identified at many levels. Identifying genetic variation is possible from observations of phenotypic variation in either quantitative traits (traits that vary continuously and are coded for by many genes, e.g., leg length in dogs) or discrete traits (traits that fall into discrete categories and are coded for by one or a few genes, e.g., white, pink, or red petal color ...

  3. Heredity - Wikipedia

    en.wikipedia.org/wiki/Heredity

    Heredity, also called inheritance or biological inheritance, is the passing on of traits from parents to their offspring; either through asexual reproduction or sexual reproduction, the offspring cells or organisms acquire the genetic information of their parents.

  4. Genetics - Wikipedia

    en.wikipedia.org/wiki/Genetics

    Genetics is the study of genes, genetic variation, and heredity in organisms. [1] [2] [3] It is an important branch in biology because heredity is vital to organisms' evolution. Gregor Mendel, a Moravian Augustinian friar working in the 19th century in Brno, was the first to study genetics scientifically. Mendel studied "trait inheritance ...

  5. Human genetic variation - Wikipedia

    en.wikipedia.org/wiki/Human_genetic_variation

    Genetic variation Genetic variation of Eurasian populations showing different frequency of West- and East-Eurasian components [56] It is commonly assumed that early humans left Africa, and thus must have passed through a population bottleneck before their African-Eurasian divergence around 100,000 years ago (ca. 3,000 generations).

  6. Mendelian inheritance - Wikipedia

    en.wikipedia.org/wiki/Mendelian_inheritance

    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] These principles were initially controversial.

  7. Mendelian traits in humans - Wikipedia

    en.wikipedia.org/wiki/Mendelian_traits_in_humans

    Autosomal dominant A 50/50 chance of inheritance. Sickle-cell disease is inherited in the autosomal recessive pattern. When both parents have sickle-cell trait (carrier), a child has a 25% chance of sickle-cell disease (red icon), 25% do not carry any sickle-cell alleles (blue icon), and 50% have the heterozygous (carrier) condition. [1]

  8. Introduction to genetics - Wikipedia

    en.wikipedia.org/wiki/Introduction_to_genetics

    This variation is probably due to a large number of alleles, each changing the risk a little bit. [17] Several of the genes have been identified, such as BRCA1 and BRCA2 , but not all of them. However, although some of the risks are genetic, the risk of this cancer is also increased by being overweight, heavy alcohol consumption and not ...

  9. Outline of genetics - Wikipedia

    en.wikipedia.org/wiki/Outline_of_genetics

    The following outline is provided as an overview of and topical guide to genetics: . Genetics – science of genes, heredity, and variation in living organisms. [1] [2] Genetics deals with the molecular structure and function of genes, and gene behavior in context of a cell or organism (e.g. dominance and epigenetics), patterns of inheritance from parent to offspring, and gene distribution ...