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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] For a gene that exists in two alleles, the Hardy–Weinberg equation states that (p 2) + (2pq) + (q 2) = 1. If we apply this equation to our flower color gene, then
The allele frequency spectrum can be written as the vector = (,,,,), where is the number of observed sites with derived allele frequency .In this example, the observed allele frequency spectrum is (,,,,), due to four instances of a single observed derived allele at a particular SNP loci, two instances of two derived alleles, and so on.
This example illustrates that one can sometimes increase the N50 length simply by removing some of the shortest contigs or scaffolds from an assembly. If the estimated or known size of the genome from the fictional species A is 500 kbp then the NG50 contig length is 30 kbp because 80 + 70 + 50 + 40 + 30 is greater than 50% of 500.
Using the example gene effects (white label "9" in the diagram), this mean is = 37.87. The equivalent mean in the dispersed bulk is 36.94 (black label "10"), which is depressed by the amount 0.93. This is the inbreeding depression from this Genetic Drift.
A diagram of DNA base pairing, demonstrating the basis for Chargaff's rules. Chargaff's rules (given by Erwin Chargaff) state that in the DNA of any species and any organism, the amount of guanine should be equal to the amount of cytosine and the amount of adenine should be equal to the amount of thymine.
where is the number of segregating sites (an example of a segregating site would be a single-nucleotide polymorphism) in the sample and = = is the () th harmonic number. This estimate is based on coalescent theory. Watterson's estimator is commonly used for its simplicity.
The proportion of segregating sites within a gene is an important statistic in population genetics since it can be used to estimate mutation rate assuming no selection. For example it is used to calculate the Tajima's D neutral evolution statistic. A sequence alignment, produced by ClustalO, of mammalian histone proteins.
Ab Initio gene prediction is an intrinsic method based on gene content and signal detection. Because of the inherent expense and difficulty in obtaining extrinsic evidence for many genes, it is also necessary to resort to ab initio gene finding, in which the genomic DNA sequence alone is systematically searched for certain tell-tale signs of protein-coding genes.