Next Generation DNA Sequencing and Its Application in Clinical Medicine.
10.14734/kjp.2014.25.3.133
- Author:
Sechin CHO
1
Author Information
1. University of Kansas School of Medicine, Wichita, Kansas, USA. cho3gene@gmail.com
- Publication Type:Review
- Keywords:
New generation DNA sequencing;
Whole genome/exome sequencing;
Human genetic disease
- MeSH:
Anniversaries and Special Events;
Clinical Coding;
Clinical Medicine*;
DNA;
DNA, Mitochondrial;
Education;
Genetic Code;
Genetics;
Genetics, Medical;
Genome;
Genome, Human;
Genomics;
Human Genome Project;
Humans;
Missions and Missionaries;
Nucleotides;
Sequence Analysis, DNA*
- From:Korean Journal of Perinatology
2014;25(3):133-139
- CountryRepublic of Korea
- Language:English
-
Abstract:
Watson and Crick published a paper on the double helical structure of DNA in Nature in April 25, 1953. The human genome is contained in the 23 pairs of chromosomes and in the mitochondrial DNA of each cell. The Human Genome Project was launched in 1990 under the direction of Watson and concluded in 2003, on the 50th anniversary of Watson and Crick paper. Over 6 billion of nucleotides of genetic codes are in single cells. There are 23,000 protein coding genes and the remainder are non-coding DNA, regulatory DNA. Since the completion of Human Genome Project, these huge genomic information has been translated into clinically usable medical information. With the advent of massively parallel DNA sequencing, known as next generation DNA sequencing, the cost and turn-around time were significantly reduced so that the era of Whole Genome Sequencing entered into hospitals and medical clinics. On June 16, 2014 American Society of Human Genetics revised its mission statement as follows. "Our mission is to advance human genetics in science, health and society through research, education and advocacy". Finally medical genetics nestled its roots in the midst of genetics and genomics.
