Why is The Detection of DNA Sequences Important?

Abdul M Gbaj
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Abdul M Gbaj: Department of Medicinal Chemistry, Faculty of Pharmacy, University of Tripoli, Libya

Novel Approaches in Drug Designing & Development, 2018, vol. 4, issue 1, 8-9

Abstract: Now that sequencing of the human genome is finished [1,2], much information on the underlying genetic causes of many inherited and acquired diseases has been made available. Many genetic diseases have been found to be the result of a change of a single base pair. These alterations, termed single nucleotide polymorphisms (SNP), may cause changes in the amino acid sequence of important proteins. Some SNPs on the other hand may not cause a change in protein expression but may be close on the chromosome to other unknown deleterious mutations and can thus serve as genetic markers for these.

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Date: 2018
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Persistent link: https://EconPapers.repec.org/RePEc:adp:jnapdd:v:4:y:2018:i:1:p:8-9

DOI: 10.19080/NAPDD.2018.04.555628

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