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  2. Pedigree chart - Wikipedia

    en.wikipedia.org/wiki/Pedigree_chart

    It may be used to discover where the genes in question are located (x, y, or autosome chromosome), and to determine whether a trait is dominant or recessive. When a pedigree shows a condition appearing in a 50:50 ratio between men and women, it is considered autosomal.

  3. Hardy–Weinberg principle - Wikipedia

    en.wikipedia.org/wiki/Hardy–Weinberg_principle

    Length of p, q corresponds to allele frequencies (here p = 0.6, q = 0.4). Then area of rectangle represents genotype frequencies (thus AA : Aa : aa = 0.36 : 0.48 : 0.16 ). The different ways to form genotypes for the next generation can be shown in a Punnett square , where the proportion of each genotype is equal to the product of the row and ...

  4. Dominance (genetics) - Wikipedia

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

    Thus, allele R is dominant over allele r, and allele r is recessive to allele R. [4] Dominance is not inherent to an allele or its traits . It is a strictly relative effect between two alleles of a given gene of any function; one allele can be dominant over a second allele of the same gene, recessive to a third, and co-dominant with a fourth.

  5. Genotype - Wikipedia

    en.wikipedia.org/wiki/Genotype

    Since each parent must have a copy of the recessive allele in order to have an affected offspring, the parents are referred to as carriers of the condition. [ 11 ] [ 12 ] [ 13 ] In autosomal conditions, the sex of the offspring does not play a role in their risk of being affected.

  6. Genotype frequency - Wikipedia

    en.wikipedia.org/wiki/Genotype_frequency

    if the allele A frequency is denoted by the symbol p and the allele a frequency denoted by q, then p+q=1. For example, if p=0.7, then q must be 0.3. In other words, if the allele frequency of A equals 70%, the remaining 30% of the alleles must be a, because together they equal 100%. [5]

  7. Simple Mendelian genetics in humans - Wikipedia

    en.wikipedia.org/wiki/Simple_Mendelian_genetics...

    According to the model of Mendelian inheritance, alleles may be dominant or recessive, one allele is inherited from each parent, and only those who inherit a recessive allele from each parent exhibit the recessive phenotype. Offspring with either one or two copies of the dominant allele will display the dominant phenotype.

  8. 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.

  9. Classical genetics - Wikipedia

    en.wikipedia.org/wiki/Classical_genetics

    The alleles of genes can either be dominant or recessive. A dominant allele needs only one copy to be expressed while a recessive allele needs two copies (homozygous) in a diploid organism to be expressed. Dominant and recessive alleles help to determine the offspring's genotypes, and therefore phenotypes. [citation needed]