Application of Next-generation Sequencing in Clinical Molecular Diagnostics

被引:3
|
作者
Seifi, Morteza [1 ]
Ghasemi, Asghar [2 ]
Raeisi, Sina [3 ]
Heidarzadeh, Siamak [4 ]
机构
[1] Univ Alberta, Fac Med & Dent, Dept Med Genet, Edmonton, AB, Canada
[2] Univ Tehran Med Sci, Sch Med, Dept Clin Biochem, Tehran, Iran
[3] Tabriz Univ Med Sci, Fac Med, Dept Biochem & Clin Labs, Tabriz, Iran
[4] Univ Tehran Med Sci, Sch Publ Hlth, Dept Pathobiol, Tehran, Iran
关键词
Bioinformatics; clinical molecular applications; ethical aspects; next generation sequencing; INCIDENTAL FINDINGS; DNA METHYLATION; COPY-NUMBER; GENOME; CHROMATIN; CANCER; EXOME; CELLS; RECOMMENDATIONS; EPIGENETICS;
D O I
10.1590/1678-4324-2017160414
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Next-generation sequencing (NGS) is the catch all terms that used to explain several different modern sequencing technologies which let us to sequence nucleic acids much more rapidly and cheaply than the formerly used Sanger sequencing, and as such have revolutionized the study of molecular biology and genomics with excellent resolution and accuracy. Over the past years, many academic companies and institutions have continued technological advances to expand NGS applications from research to the clinic. In this review, the performance and technical features of current NGS platforms were described. Furthermore, advances in the applying of NGS technologies towards the progress of clinical molecular diagnostics were emphasized. General advantages and disadvantages of each sequencing system are summarized and compared to guide the selection of NGS platforms for specific research aims.
引用
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页数:15
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