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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. 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. 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.

  5. Homologous recombination - Wikipedia

    en.wikipedia.org/wiki/Homologous_recombination

    Homologous recombination is a type of genetic recombination in which genetic information is exchanged between two similar or identical molecules of double-stranded or single-stranded nucleic acids (usually DNA as in cellular organisms but may be also RNA in viruses).

  6. Sequence homology - Wikipedia

    en.wikipedia.org/wiki/Sequence_homology

    Homology among DNA, RNA, or proteins is typically inferred from their nucleotide or amino acid sequence similarity. Significant similarity is strong evidence that two sequences are related by evolutionary changes from a common ancestral sequence. Alignments of multiple sequences are used to indicate which regions of each sequence are homologous.

  7. Gene - Wikipedia

    en.wikipedia.org/wiki/Gene

    The total number of protein-coding genes (the Earth's proteome) is estimated to be 5 million sequences. [98] Although the number of base-pairs of DNA in the human genome has been known since the 1950s, the estimated number of genes has changed over time as definitions of genes, and methods of detecting them have been refined.

  8. Polyploidy - Wikipedia

    en.wikipedia.org/wiki/Polyploidy

    This image shows haploid (single), diploid (double), triploid (triple), and tetraploid (quadruple) sets of chromosomes. Triploid and tetraploid chromosomes are examples of polyploidy. Polyploidy is a condition in which the cells of an organism have more than two paired sets of ( homologous ) chromosomes .

  9. Homology directed repair - Wikipedia

    en.wikipedia.org/wiki/Homology_directed_repair

    This action by the MRN complex may prevent chromosomal breaks. At some later point the DNA ends are processed so that unnecessary residuals of chemical groups are removed and single strand overhangs are formed. Meanwhile, from the beginning, every piece of single stranded DNA is covered by the protein RPA (Replication Protein A).