Literature DB >> 23631825

Translational utility of next-generation sequencing.

Frank S Ong1, Jimmy C Lin, Kingshuk Das, Daniel S Grosu, Jian-Bing Fan.   

Abstract

The development of next-generation sequencing (NGS) technology has made DNA sequencing not only rapid and cost-effective, but also highly accurate and reproducible. The translational utility of genomic sequencing is clear, from understanding of human genetic variation and its association with disease risk and individual response to treatment, to the interpretation and translation of the data for clinical decision making. It will be a critical technology for disease characterization and monitoring in molecular pathology and is expected to become a central piece of routine healthcare management which will result in accurate and reliable reporting, a prerequisite for physicians to practice genomic medicine.
Copyright © 2013 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Cancer genome sequencing; Clinical sequencing; NGS; NIPT; Next-generation sequencing; Non-invasive diagnosis

Mesh:

Year:  2013        PMID: 23631825     DOI: 10.1016/j.ygeno.2013.04.012

Source DB:  PubMed          Journal:  Genomics        ISSN: 0888-7543            Impact factor:   5.736


  10 in total

1.  Cytogenetic Analysis of the Products of Conception After Spontaneous Abortion in the First Trimester.

Authors:  Xueluo Zhang; Junmei Fan; Yanhua Chen; Jun Wang; Zhijiao Song; Jinghui Zhao; Zhongyun Li; Xueqing Wu; Yuanjing Hu
Journal:  Cytogenet Genome Res       Date:  2021-05-11       Impact factor: 1.636

2.  Next Generation sequencing is the impetus for the next generation of laboratory-based genetic counselors.

Authors:  Amy Swanson; Erica Ramos; Holly Snyder
Journal:  J Genet Couns       Date:  2014-01-17       Impact factor: 2.537

3.  Clinical integration of next generation sequencing: coverage and reimbursement challenges.

Authors:  Patricia A Deverka; Jennifer C Dreyfus
Journal:  J Law Med Ethics       Date:  2014       Impact factor: 1.718

Review 4.  Care delivery considerations for widespread and equitable implementation of inherited cancer predisposition testing.

Authors:  Deborah Cragun; Anita Y Kinney; Tuya Pal
Journal:  Expert Rev Mol Diagn       Date:  2016-12-13       Impact factor: 5.225

5.  Developing a genomics rotation: Practical training around variant interpretation for genetic counseling students.

Authors:  Megan E Grove; Shana White; Dianna G Fisk; Shannon Rego; Orit Dagan-Rosenfeld; Jennefer N Kohler; Chloe M Reuter; Devon Bonner; Matthew T Wheeler; Jonathan A Bernstein; Kelly E Ormond; Andrea K Hanson-Kahn
Journal:  J Genet Couns       Date:  2019-02-01       Impact factor: 2.537

6.  Non-invasive Analysis of Genomic Copy Number Variation in Patients with Hepatocellular Carcinoma by Next Generation DNA Sequencing.

Authors:  Hongtao Xu; Xia Zhu; Zulong Xu; Yue Hu; Shiping Bo; Tongjing Xing; Kuichun Zhu
Journal:  J Cancer       Date:  2015-01-18       Impact factor: 4.207

7.  Genetic variation among 82 pharmacogenes: The PGRNseq data from the eMERGE network.

Authors:  W S Bush; D R Crosslin; A Owusu-Obeng; J Wallace; B Almoguera; M A Basford; S J Bielinski; D S Carrell; J J Connolly; D Crawford; K F Doheny; C J Gallego; A S Gordon; B Keating; J Kirby; T Kitchner; S Manzi; A R Mejia; V Pan; C L Perry; J F Peterson; C A Prows; J Ralston; S A Scott; A Scrol; M Smith; S C Stallings; T Veldhuizen; W Wolf; S Volpi; K Wiley; R Li; T Manolio; E Bottinger; M H Brilliant; D Carey; R L Chisholm; C G Chute; J L Haines; H Hakonarson; J B Harley; I A Holm; I J Kullo; G P Jarvik; E B Larson; C A McCarty; M S Williams; J C Denny; L J Rasmussen-Torvik; D M Roden; M D Ritchie
Journal:  Clin Pharmacol Ther       Date:  2016-06-01       Impact factor: 6.875

8.  Clinical and genomic evaluation of a Chinese patient with a novel deletion associated with Phelan-McDermid syndrome.

Authors:  Dongzhu Lei; Shaoyuan Li; Santasree Banerjee; Haoqing Zhang; Caiyun Li; Shuai Hou; Danjing Chen; Haiying Yan; Hanmei Li; Huan Huan Peng; Saijun Liu; Xinxin Zhang; Zhiyu Peng; Jian Wang; Huanming Yang; Hui Huang; Jing Wu
Journal:  Oncotarget       Date:  2016-12-06

Review 9.  Genetic testing for nephrotic syndrome and FSGS in the era of next-generation sequencing.

Authors:  Elizabeth J Brown; Martin R Pollak; Moumita Barua
Journal:  Kidney Int       Date:  2014-03-05       Impact factor: 10.612

10.  A visual and curatorial approach to clinical variant prioritization and disease gene discovery in genome-wide diagnostics.

Authors:  Regis A James; Ian M Campbell; Edward S Chen; Philip M Boone; Mitchell A Rao; Matthew N Bainbridge; James R Lupski; Yaping Yang; Christine M Eng; Jennifer E Posey; Chad A Shaw
Journal:  Genome Med       Date:  2016-02-02       Impact factor: 11.117

  10 in total

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