Literature DB >> 28782984

Review of Clinical Next-Generation Sequencing.

Sophia Yohe1, Bharat Thyagarajan1.   

Abstract

CONTEXT: - Next-generation sequencing (NGS) is a technology being used by many laboratories to test for inherited disorders and tumor mutations. This technology is new for many practicing pathologists, who may not be familiar with the uses, methodology, and limitations of NGS.
OBJECTIVE: - To familiarize pathologists with several aspects of NGS, including current and expanding uses; methodology including wet bench aspects, bioinformatics, and interpretation; validation and proficiency; limitations; and issues related to the integration of NGS data into patient care. DATA SOURCES: - The review is based on peer-reviewed literature and personal experience using NGS in a clinical setting at a major academic center.
CONCLUSIONS: - The clinical applications of NGS will increase as the technology, bioinformatics, and resources evolve to address the limitations and improve quality of results. The challenge for clinical laboratories is to ensure testing is clinically relevant, cost-effective, and can be integrated into clinical care.

Entities:  

Mesh:

Year:  2017        PMID: 28782984     DOI: 10.5858/arpa.2016-0501-RA

Source DB:  PubMed          Journal:  Arch Pathol Lab Med        ISSN: 0003-9985            Impact factor:   5.534


  78 in total

Review 1.  Genetic testing for hereditary gastrointestinal cancer syndromes: Interpreting results in today's practice.

Authors:  Jacquelyn M Powers; Jessica E Ebrahimzadeh; Bryson W Katona
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2.  Next-generation sequencing capacity and capabilities within the National Animal Health Laboratory Network.

Authors:  Beth Harris; Jessica Hicks; Melanie Prarat; Susan Sanchez; Beate Crossley
Journal:  J Vet Diagn Invest       Date:  2020-07-01       Impact factor: 1.279

3.  Whole exome sequencing in molecular diagnostics of cancer decreases over time: evidence from a cost analysis in the French setting.

Authors:  I Borget; J Bonastre; Arnaud Bayle; N Droin; B Besse; Z Zou; Y Boursin; S Rissel; E Solary; L Lacroix; E Rouleau
Journal:  Eur J Health Econ       Date:  2021-03-25

4.  Getting personal with myelodysplastic syndromes: is now the right time?

Authors:  Nora Chokr; Alexander B Pine; Jan Philipp Bewersdorf; Rory M Shallis; Maximilian Stahl; Amer M Zeidan
Journal:  Expert Rev Hematol       Date:  2019-04-12       Impact factor: 2.929

Review 5.  What is the potential of nanolock- and nanocross-nanopore technology in cancer diagnosis?

Authors:  Li-Qun Gu; Kent S Gates; Michael X Wang; Guangfu Li
Journal:  Expert Rev Mol Diagn       Date:  2017-12-01       Impact factor: 5.225

6.  Rapid detection and genotyping of ALK fusion variants by adapter multiplex PCR and high-resolution melting analysis.

Authors:  Mei Li; Shen Lu; Xu Sun
Journal:  Lab Invest       Date:  2019-10-22       Impact factor: 5.662

7.  Integrated transcriptomic-genomic tool Texomer profiles cancer tissues.

Authors:  Fang Wang; Shaojun Zhang; Tae-Beom Kim; Yu-Yu Lin; Ramiz Iqbal; Zixing Wang; Vakul Mohanty; Kanishka Sircar; Jose A Karam; Michael C Wendl; Funda Meric-Bernstam; John N Weinstein; Li Ding; Gordon B Mills; Ken Chen
Journal:  Nat Methods       Date:  2019-04-15       Impact factor: 28.547

8.  Two novel ANK1 loss-of-function mutations in Chinese families with hereditary spherocytosis.

Authors:  Lili Hao; Shanshan Li; Duan Ma; Shiyu Chen; Bowen Zhang; Deyong Xiao; Jin Zhang; Nan Jiang; Shayi Jiang; Jing Ma
Journal:  J Cell Mol Med       Date:  2019-04-23       Impact factor: 5.310

Review 9.  Approaches to characterize the transcriptional trajectory of human myogenesis.

Authors:  HoTae Lim; In Young Choi; Sang-Hwan Hyun; Hyesoo Kim; Gabsang Lee
Journal:  Cell Mol Life Sci       Date:  2021-02-15       Impact factor: 9.261

Review 10.  Newly identified T cell subsets in mechanistic studies of food immunotherapy.

Authors:  Vanitha Sampath; Kari C Nadeau
Journal:  J Clin Invest       Date:  2019-04-01       Impact factor: 14.808

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