Use of an Integrated Pan-Cancer Oncology Enrichment Next-Generation Sequencing Assay to Measure Tumour Mutational Burden and Detect Clinically Actionable Variants (vol 24, pg 339, 2020)

被引：0
|
作者：
Pestinger, Valerie [1 ]
Smith, Matthew [2 ]
Sillo, Toju [1 ]
Findlay, John M. [3 ]
Laes, Jean-Francois [4 ]
Martin, Gerald [5 ]
Middleton, Gary [6 ]
Taniere, Phillipe [2 ]
Beggs, Andrew D. [1 ,2 ]
机构：
[1] Univ Birmingham, Surg Res Lab, Inst Canc & Genom Sci, Vincent Dr, Birmingham B15 2TT, W Midlands, England
[2] Queen Elizabeth Hosp Birmingham, Birmingham, W Midlands, England
[3] Northern Devon Healthcare NHS Trust, Barnstaple, England
[4] OncoDNA, Gosselies, Belgium
[5] PierianDx, St Louis, MO USA
[6] Univ Birmingham, Inst Immunol & Immunotherapy, Birmingham, W Midlands, England
来源：
MOLECULAR DIAGNOSIS & THERAPY | 2020年 / 24卷 / 04期
基金：
英国医学研究理事会;
关键词：
D O I：
10.1007/s40291-020-00479-2
中图分类号：
Q3 [遗传学];
学科分类号：
071007 ; 090102 ;
摘要：
This article was originally published under a [CC BY NC 4.0] license.
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收藏
页码：505 / 505
页数：1
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