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Mutations in single nucleotide polymorphisms (SNPs - different variant positions (1%) from human genomes) are responsible for some genetic diseases. As a consequence, obtaining all SNPs from human populations is one of the primary goals of recent studies in human genomics. Two sequences of mentioned SNPs in diploid human organisms are called haplotypes. In this paper, we study haplotype reconstruction...
Most positions of the human genome are typically invariant (99%) and only some positions (1%) are commonly variant which are associated with complex genetic diseases. Haplotype reconstruction is to divide aligned SNP fragments, which is the most frequent form of difference to address genetic diseases, into two classes, and thus inferring a pair of haplotypes from them. Minimum error correction (MEC)...
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