Literature DB >> 21463242

Next-generation sequencing and its applications in molecular diagnostics.

Zhenqiang Su1, Baitang Ning, Hong Fang, Huixiao Hong, Roger Perkins, Weida Tong, Leming Shi.   

Abstract

DNA sequencing is a powerful approach for decoding a number of human diseases, including cancers. The advent of next-generation sequencing (NGS) technologies has reduced sequencing cost by orders of magnitude and significantly increased the throughput, making whole-genome sequencing a possible way for obtaining global genomic information about patients on whom clinical actions may be taken. However, the benefits offered by NGS technologies come with a number of challenges that must be adequately addressed before they can be transformed from research tools to routine clinical practices. This article provides an overview of four commonly used NGS technologies from Roche Applied Science//454 Life Sciences, Illumina, Life Technologies and Helicos Biosciences. The challenges in the analysis of NGS data and their potential applications in clinical diagnosis are also discussed.

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Year:  2011        PMID: 21463242     DOI: 10.1586/erm.11.3

Source DB:  PubMed          Journal:  Expert Rev Mol Diagn        ISSN: 1473-7159            Impact factor:   5.225


  46 in total

Review 1.  Next-generation and whole-genome sequencing in the diagnostic clinical microbiology laboratory.

Authors:  W M Dunne; L F Westblade; B Ford
Journal:  Eur J Clin Microbiol Infect Dis       Date:  2012-06-08       Impact factor: 3.267

2.  Simultaneous digital quantification and fluorescence-based size characterization of massively parallel sequencing libraries.

Authors:  Matthew T Laurie; Jessica A Bertout; Sean D Taylor; Joshua N Burton; Jay A Shendure; Jason H Bielas
Journal:  Biotechniques       Date:  2013-08       Impact factor: 1.993

3.  Genes of susceptibility to early neurodegenerative changes in the rat retina and brain: analysis by means of congenic strains.

Authors:  Elena E Korbolina; Anna A Zhdankina; Anzhela Zh Fursova; Oyuna S Kozhevnikova; Natalia G Kolosova
Journal:  BMC Genet       Date:  2016-12-22       Impact factor: 2.797

4.  Application of quantitative trait locus mapping and transcriptomics to studies of the senescence-accelerated phenotype in rats.

Authors:  Elena E Korbolina; Nikita I Ershov; Leonid O Bryzgalov; Natalia G Kolosova
Journal:  BMC Genomics       Date:  2014-12-19       Impact factor: 3.969

5.  Next generation sequencing in cardiovascular diseases.

Authors:  Francesca Faita; Cecilia Vecoli; Ilenia Foffa; Maria Grazia Andreassi
Journal:  World J Cardiol       Date:  2012-10-26

6.  Development of a protease-resistant reporter to quantify BCR-ABL activity in intact cells.

Authors:  Angela Proctor; Imola G Zigoneanu; Qunzhao Wang; Christopher E Sims; David S Lawrence; Nancy L Allbritton
Journal:  Analyst       Date:  2016-10-17       Impact factor: 4.616

Review 7.  Current evidence for an inherited genetic basis of childhood acute lymphoblastic leukemia.

Authors:  Kevin Y Urayama; Anand P Chokkalingam; Atsushi Manabe; Shuki Mizutani
Journal:  Int J Hematol       Date:  2012-12-13       Impact factor: 2.490

8.  Current and emerging technology approaches in genomics.

Authors:  Yvette P Conley; Leslie G Biesecker; Stephen Gonsalves; Carrie J Merkle; Maggie Kirk; Bradley E Aouizerat
Journal:  J Nurs Scholarsh       Date:  2013-01-07       Impact factor: 3.176

9.  Next generation sequencing for profiling expression of miRNAs: technical progress and applications in drug development.

Authors:  Jie Liu; Steven F Jennings; Weida Tong; Huixiao Hong
Journal:  J Biomed Sci Eng       Date:  2011-10

Review 10.  DNA markers in molecular diagnostics for hepatocellular carcinoma.

Authors:  Ying-Hsiu Su; Selena Y Lin; Wei Song; Surbhi Jain
Journal:  Expert Rev Mol Diagn       Date:  2014-08-07       Impact factor: 5.225

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