Genome sequencing includes methods and technologies that are used
for determining the order of nucleotides (A, T, C or G) along a DNA
sequence. A single nucleotide polymorphism or SNP is a DNA sequence
variation occurring when a single nucleotide in the genome differs within
population members. Initially, we consider a particular site under a model
where there are just two possible alleles. The following results can be then
adapted to the case in which all four possible alleles (variants) may occur.
The most common (rare) allele is termed the major (minor) allele respectively.