Medical Research on Genomics.

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Genetic disorders affect approximately six percent of all newborns worldwide (Moss, 2006). These disorders range from benign recessive disorders to life-threatening conditions which may result in a high mortality rate. To combat these disorders, prior tests need to be carried out in advance to detect the presence of the disorder which may manifest in a disarrangement of the genetic code or even the absence of a crucial part of the genetic code commonly known as deletions. DNA sequencing is one of the critical tests performed to test for genetic disorders. Three commonly used methods in DNA sequencing include exome sequencing, whole-genome sequencing and SNP array (GHR, 2019).

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