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  2. Autosome - Wikipedia

    en.wikipedia.org/wiki/Autosome

    Autosomal genetic disorders can arise due to a number of causes, some of the most common being nondisjunction in parental germ cells or Mendelian inheritance of deleterious alleles from parents. Autosomal genetic disorders which exhibit Mendelian inheritance can be inherited either in an autosomal dominant or recessive fashion. [ 7 ]

  3. Genealogical DNA test - Wikipedia

    en.wikipedia.org/wiki/Genealogical_DNA_test

    Like autosomal DNA, X-chromosome DNA undergoes random recombination at each generation (except for father-to-daughter X-chromosomes, which are passed down unchanged). There are specialized inheritance charts which describe the possible patterns of X-chromosome DNA inheritance for males and females.

  4. Genetic genealogy - Wikipedia

    en.wikipedia.org/wiki/Genetic_genealogy

    e. Genetic genealogy is the use of genealogical DNA tests, i.e., DNA profiling and DNA testing, in combination with traditional genealogical methods, to infer genetic relationships between individuals. This application of genetics came to be used by family historians in the 21st century, as DNA tests became affordable.

  5. Human genetics - Wikipedia

    en.wikipedia.org/wiki/Human_genetics

    Autosomal recessive inheritance, a 25% chance. Autosomal recessive traits is one pattern of inheritance for a trait, disease, or disorder to be passed on through families. For a recessive trait or disease to be displayed two copies of the trait or disorder needs to be presented. The trait or gene will be located on a non-sex chromosome.

  6. Heredity - Wikipedia

    en.wikipedia.org/wiki/Heredity

    An example pedigree chart of an autosomal dominant disorder An example pedigree chart of an autosomal recessive disorder An example pedigree chart of a sex-linked disorder (The gene is on the X chromosome.) The description of a mode of biological inheritance consists of three main categories: 1. Number of involved loci

  7. Punnett square - Wikipedia

    en.wikipedia.org/wiki/Punnett_square

    The Punnett square is a visual representation of Mendelian inheritance, a fundamental concept in genetics discovered by Gregor Mendel. [10] For multiple traits, using the "forked-line method" is typically much easier than the Punnett square. Phenotypes may be predicted with at least better-than-chance accuracy using a Punnett square, but the ...

  8. Mendelian inheritance - Wikipedia

    en.wikipedia.org/wiki/Mendelian_inheritance

    e. 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.

  9. FamilyTreeDNA - Wikipedia

    en.wikipedia.org/wiki/FamilyTreeDNA

    FamilyTreeDNA offers analysis of autosomal DNA, Y-DNA, and mitochondrial DNA to individuals for genealogical purpose. With a database of more than two million records, it is the most popular company worldwide for Y-DNA and mitochondrial DNA, and the fourth most popular for autosomal DNA. In Europe, it is the most common also for autosomal DNA.

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