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  2. Genotype - Wikipedia

    en.wikipedia.org/wiki/Genotype

    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. In diploid species like humans, two full sets of ...

  3. Epigenetics - Wikipedia

    en.wikipedia.org/wiki/Epigenetics

    Epigenetic mechanisms. In biology, epigenetics is the study of heritable traits, or a stable change of cell function, that happen without changes to the DNA sequence. [1] The Greek prefix epi-(ἐπι-"over, outside of, around") in epigenetics implies features that are "on top of" or "in addition to" the traditional (DNA sequence based) genetic mechanism of inheritance. [2]

  4. Allele - Wikipedia

    en.wikipedia.org/wiki/Allele

    A null allele is a gene variant that lacks the gene's normal function because it either is not expressed, or the expressed protein is inactive. For example, at the gene locus for the ABO blood type carbohydrate antigens in humans, [13] classical genetics recognizes three alleles, I A, I B, and i, which determine compatibility of blood transfusions.

  5. Genetic marker - Wikipedia

    en.wikipedia.org/wiki/Genetic_marker

    Genetic markers can be used to study the relationship between an inherited disease and its genetic cause (for example, a particular mutation of a gene that results in a defective protein). It is known that pieces of DNA that lie near each other on a chromosome tend to be inherited together.

  6. Genomic imprinting - Wikipedia

    en.wikipedia.org/wiki/Genomic_imprinting

    As of 2019, 260 imprinted genes have been reported in mice and 228 in humans. [10] Genomic imprinting is an inheritance process independent of the classical Mendelian inheritance. [11] It is an epigenetic process that involves DNA methylation and histone methylation without altering the genetic sequence.

  7. Molecular phylogenetics - Wikipedia

    en.wikipedia.org/wiki/Molecular_phylogenetics

    Molecular phylogenetics (/ m ə ˈ l ɛ k j ʊ l ər ˌ f aɪ l oʊ dʒ ə ˈ n ɛ t ɪ k s, m ɒ-, m oʊ-/ [1] [2]) is the branch of phylogeny that analyzes genetic, hereditary molecular differences, predominantly in DNA sequences, to gain information on an organism's evolutionary relationships. From these analyses, it is possible to determine ...

  8. Evolution - Wikipedia

    en.wikipedia.org/wiki/Evolution

    Evolution is the change in the heritable characteristics of biological populations over successive generations. [1] [2] It occurs when evolutionary processes such as natural selection and genetic drift act on genetic variation, resulting in certain characteristics becoming more or less common within a population over successive generations. [3]

  9. Gene family - Wikipedia

    en.wikipedia.org/wiki/Gene_family

    If the genes of a gene family encode proteins, the term protein family is often used in an analogous manner to gene family. The expansion or contraction of gene families along a specific lineage can be due to chance, or can be the result of natural selection. [2] To distinguish between these two cases is often difficult in practice.