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  2. Chromosomal crossover - Wikipedia

    en.wikipedia.org/wiki/Chromosomal_crossover

    If two genes are located close together on a chromosome, the likelihood that a recombination event will separate these two genes is less than if they were farther apart. Genetic linkage describes the tendency of genes to be inherited together as a result of their location on the same chromosome.

  3. Genealogical DNA test - Wikipedia

    en.wikipedia.org/wiki/Genealogical_DNA_test

    The Y-chromosome is one of the 23rd pair of human chromosomes. Only males have a Y-chromosome, because women have two X chromosomes in their 23rd pair. A man's patrilineal ancestry, or male-line ancestry, can be traced using the DNA on his Y-chromosome (Y-DNA), because the Y-chromosome is transmitted from a father to son nearly unchanged. [31]

  4. Human genetic variation - Wikipedia

    en.wikipedia.org/wiki/Human_genetic_variation

    The human genome has a total length of approximately 3.2 billion base pairs (bp) in 46 chromosomes of DNA as well as slightly under 17,000 bp DNA in cellular mitochondria. In 2015, the typical difference between an individual's genome and the reference genome was estimated at 20 million base pairs (or 0.6% of the total). [ 2 ]

  5. Genetic linkage - Wikipedia

    en.wikipedia.org/wiki/Genetic_linkage

    Genetic linkage is the tendency of DNA sequences that are close together on a chromosome to be inherited together during the meiosis phase of sexual reproduction.Two genetic markers that are physically near to each other are unlikely to be separated onto different chromatids during chromosomal crossover, and are therefore said to be more linked than markers that are far apart.

  6. Human genome - Wikipedia

    en.wikipedia.org/wiki/Human_genome

    HEXA gene (on chromosome 15) Canavan disease: 2.5% Eastern European Jewish ancestry ASPA gene (on chromosome 17) Familial dysautonomia: 600 known cases worldwide since discovery IKBKAP gene (on chromosome 9) Fragile X syndrome: 1.4:10000 in males, 0.9:10000 in females FMR1 gene (on X chromosome) Mucolipidosis type IV: 1:90 to 1:100 in Ashkenazi ...

  7. Genetic genealogy - Wikipedia

    en.wikipedia.org/wiki/Genetic_genealogy

    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.

  8. Genetics - Wikipedia

    en.wikipedia.org/wiki/Genetics

    This is an accepted version of this page This is the latest accepted revision, reviewed on 28 January 2025. Science of genes, heredity, and variation in living organisms This article is about the general scientific term. For the scientific journal, see Genetics (journal). For a more accessible and less technical introduction to this topic, see Introduction to genetics. For the Meghan Trainor ...

  9. Genome - Wikipedia

    en.wikipedia.org/wiki/Genome

    Eukaryotic genomes are composed of one or more linear DNA chromosomes. The number of chromosomes varies widely from Jack jumper ants and an asexual nemotode, [28] which each have only one pair, to a fern species that has 720 pairs. [29] It is surprising the amount of DNA that eukaryotic genomes contain compared to other genomes.