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Clinical massively parallel next-generation sequencing analysis of 409 cancer-related genes for mutations and copy number variations in solid tumours

机译：临床大规模并行下一代测序分析的409个癌症相关基因在实体瘤中的突变和拷贝数变异

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摘要

Background: In a clinical diagnostic laboratory, we evaluated the applicability of the Ion Proton sequencer for screening 409 cancer-related genes in solid tumours.

机译：背景：在临床诊断实验室中，我们评估了离子质子测序仪在实体瘤中筛选409个与癌症相关的基因的适用性。

著录项

期刊名称 British Journal of Cancer
作者
R R Singh; K P Patel; M J Routbort; K Aldape; X Lu; J Manekia; R Abraham; N G Reddy; B A Barkoh; J Veliyathu; L J Medeiros; R Luthra;
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作者单位

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年(卷),期 2014(111),10
年度 2014
页码 2014–2023
总页数 10
原文格式 PDF
正文语种
中图分类肿瘤学;
关键词
next-generation sequencing Ion Proton Ion Torrent solid tumours mutations copy number variations;

机译：下一代测序;离子质子;离子洪流;实体瘤;突变;拷贝数变异;

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专利

1. Next-generation sequencing reveals the mutational landscape of clinically diagnosed Usher syndrome: copy number variations, phenocopies, a predominant target for translational read-through, and PEX26 mutated in Heimler syndrome [J] . Klaus Rohrschneider, Robert W. Haile, Tobias Eisenberger, Molecular Genetics & Genomic Medicine . 2017,第5期

机译：下一代测序揭示了临床诊断的Usher综合征的突变情况：拷贝数变异，表型，翻译通读的主要靶标以及在Heimler综合征中突变的PEX26
2. Next-Generation Sequencing in Gynaecological Tumours: The Prognostic and Predictive Value of the Most Common Mutations Found in Ovarian, Endometrial, and Cervical Tumours: Literature Review and the University Medical Centre Utrecht Next-Generation Sequencing Data [J] . van Winkel Eline, de Leng Wendy W. J., Witteveen Petronella O., Pathobiology: journal of immunopathology, molecular and cellular biology . 2017,第6期

机译：妇科肿瘤中的下一代测序：卵巢，子宫内膜和宫颈肿瘤中最常见的突变的预后和预测值：文献综述和大学医疗中心UTRECHT下一代测序数据
3. Clinical validation of a next-generation sequencing screen for mutational hotspots in 46 cancer-related genes [J] . SinghR.R., PatelK.P., RoutbortM.J., The Journal of molecular diagnostics: JMD . 2013,第5期

机译：下一代测序筛查46种与癌症相关基因的突变热点的临床验证
4. Mutational Analysis from Circulating Tumor Cells Using Next-Generation Sequencing [C] . Michael Schwartz, Christine Fu, Tony Tran, International Molecular Medicine Tri-Conference. . 2015

机译：利用下一代测序从循环肿瘤细胞的突变分析
5. Computational methods to identify genetic mutations from next-generation sequencing data [D] . Lee, Heewook. 2015

机译：从下一代测序数据中识别遗传突变的计算方法
6. Integration of next-generation sequencing in clinical diagnostic molecular pathology laboratories for analysis of solid tumours; an expert opinion on behalf of IQN Path ASBL [O] . Zandra C Deans, Jose Luis Costa, Ian Cree, -1

机译：将下一代测序技术整合到临床诊断分子病理学实验室中用于分析实体瘤；代表IQN Path ASBL的专家意见
7. Clinical massively parallel next-generation sequencing analysis of 409 cancer-related genes for mutations and copy number variations in solid tumours [O] . R R Singh, K P Patel, M J Routbort, 2014

机译：409个癌症相关基因的临床大规模平行的下一代测序分析，用于突变和固体肿瘤的拷贝数变化

Clinical massively parallel next-generation sequencing analysis of 409 cancer-related genes for mutations and copy number variations in solid tumours

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