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  2. Chromatid - Wikipedia

    en.wikipedia.org/wiki/Chromatid

    Chromatid pairs are normally genetically identical, and said to be homozygous. However, if mutations occur, they will present slight differences, in which case they are heterozygous . The pairing of chromatids should not be confused with the ploidy of an organism, which is the number of homologous versions of a chromosome.

  3. Gene conversion - Wikipedia

    en.wikipedia.org/wiki/Gene_conversion

    Gene conversion is the process by which one DNA sequence replaces a homologous sequence such that the sequences become identical after the conversion. [1] Gene conversion can be either allelic, meaning that one allele of the same gene replaces another allele, or ectopic, meaning that one paralogous DNA sequence converts another.

  4. Sister chromatids - Wikipedia

    en.wikipedia.org/wiki/Sister_chromatids

    A sister chromatid refers to the identical copies formed by the DNA replication of a chromosome, with both copies joined together by a common centromere. In other words, a sister chromatid may also be said to be 'one-half' of the duplicated chromosome. A pair of sister chromatids is called a dyad.

  5. Ploidy - Wikipedia

    en.wikipedia.org/wiki/Ploidy

    The haploid gametes produced by most organisms combine to form a zygote with n pairs of chromosomes, i.e. 2n chromosomes in total. The chromosomes in each pair, one of which comes from the sperm and one from the egg, are said to be homologous. Cells and organisms with pairs of homologous chromosomes are called diploid.

  6. Locus (genetics) - Wikipedia

    en.wikipedia.org/wiki/Locus_(genetics)

    Parts of a typical chromosome: (1) Chromatid (2) Centromere (3) Short (p) arm (4) Long (q) arm. In genetics, a locus (pl.: loci) is a specific, fixed position on a chromosome where a particular gene or genetic marker is located. [1]

  7. Chromosomal crossover - Wikipedia

    en.wikipedia.org/wiki/Chromosomal_crossover

    Crossing over occurs between prophase I and metaphase I and is the process where two homologous non-sister chromatids pair up with each other and exchange different segments of genetic material to form two recombinant chromosome sister chromatids. It can also happen during mitotic division, [1] which may result in loss of heterozygosity.

  8. Bivalent (genetics) - Wikipedia

    en.wikipedia.org/wiki/Bivalent_(genetics)

    A bivalent. In cellular biology, a bivalent is one pair of chromosomes (homologous chromosomes) in a tetrad.A tetrad is the association of a pair of homologous chromosomes (4 sister chromatids) physically held together by at least one DNA crossover.

  9. Polyploidy - Wikipedia

    en.wikipedia.org/wiki/Polyploidy

    Most species whose cells have nuclei are diploid, meaning they have two complete sets of chromosomes, one from each of two parents; each set contains the same number of chromosomes, and the chromosomes are joined in pairs of homologous chromosomes.