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  2. Bivalent (genetics) - Wikipedia

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

    A tetrad is the association of a pair of homologous chromosomes (4 sister chromatids) physically held together by at least one DNA crossover. This physical attachment allows for alignment and segregation of the homologous chromosomes in the first meiotic division. In most organisms, each replicated chromosome (composed of two identical sisters ...

  3. Sequence homology - Wikipedia

    en.wikipedia.org/wiki/Sequence_homology

    Sequences are either homologous or not. [3] This involves that the term "percent homology" is a misnomer. [4] As with morphological and anatomical structures, sequence similarity might occur because of convergent evolution, or, as with shorter sequences, by chance, meaning

  4. Tetrad (meiosis) - Wikipedia

    en.wikipedia.org/wiki/Tetrad_(meiosis)

    The tetrad is the four spores produced after meiosis of a yeast or other Ascomycota, Chlamydomonas or other alga, or a plant. After parent haploids mate, they produce diploids. Under appropriate environmental conditions, diploids sporulate and undergo meiosis. The meiotic products, spores, remain packaged in the parental cell body to produce ...

  5. Crossover interference - Wikipedia

    en.wikipedia.org/wiki/Crossover_interference

    Crossover interference is the term used to refer to the non-random placement of crossovers with respect to each other during meiosis.The term is attributed to Hermann Joseph Muller, who observed that one crossover "interferes with the coincident occurrence of another crossing over in the same pair of chromosomes, and I have accordingly termed this phenomenon ‘interference’."

  6. Chromosomal crossover - Wikipedia

    en.wikipedia.org/wiki/Chromosomal_crossover

    Because chromosomal regions composed of transposons have large quantities of identical, repetitious code in a condensed space, it is thought that transposon regions undergoing a crossover event are more prone to erroneous complementary match-up; [33] that is to say, a section of a chromosome containing a lot of identical sequences, should it ...

  7. 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.

  8. Genetic recombination - Wikipedia

    en.wikipedia.org/wiki/Genetic_recombination

    [citation needed] While in this formation, homologous sites on two chromatids can closely pair with one another, and may exchange genetic information. [ 6 ] Because there is a small probability of recombination at any location along a chromosome, the frequency of recombination between two locations depends on the distance separating them.

  9. Substitution matrix - Wikipedia

    en.wikipedia.org/wiki/Substitution_matrix

    To this end, we will construct a 20x20 matrix where the (,) th entry is equal to the probability of the th amino acid being transformed into the th amino acid in a certain amount of evolutionary time. There are many different ways to construct such a matrix, called a substitution matrix. Here are the most commonly used ones:

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