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Mutation Detection in Patients With Advanced Cancer by Universal Sequencing of Cancer-Related Genes in Tumor and Normal DNA vs Guideline-Based Germline Testing

机译：癌症相关基因的通用测序癌症和正常DNA癌症患者的突变检测与指南的种系检测

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Diana Mandelker; Liying Zhang; Yelena Kemel; Zsofia K. Stadler; Vijai Joseph; Ahmet Zehir; Nisha Pradhan; Angela Arnold; Michael F. Walsh; Yirong Li; Anoop R. Balakrishnan; Aijazuddin Syed; Meera Prasad; Khedoudja Nafa; Maria I. Carlo; Karen A. Cadoo; Meg Sheehan; Megan H. Fleischut; Erin Salo-Mullen; Magan Trottier; Steven M. Lipkin; Anne Lincoln; Semanti Mukherjee; Vignesh Ravichandran; Roy Cambria; Jesse Galle; Wassim Abida; Marcia E. Arcila; Ryma Benayed; Ronak Shah; Kenneth Yu; Dean F. Bajorin; Jonathan A. Coleman; Steven D. Leach; Maeve A. Lowery; Julio Garcia-Aguilar; Philip W. Kantoff; Charles L. Sawyers; Maura N. Dickler; Leonard Saltz; Robert J. Motzer; Eileen M. O’Reilly; Howard I. Scher; José Baselga; David S. Klimstra; David B. Solit; David M. Hyman; Michael F. Berger; Marc Ladanyi; Mark E. Robson; Kenneth Offit;
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1. Mutation Detection in Patients With Advanced Cancer by Universal Sequencing of Cancer-Related Genes in Tumor and Normal DNA vs Guideline-Based Germline Testing (vol 318, pg 825, 2017) [J] . Mandelker D., Zhang L., Kemel Y. JAMA: the Journal of the American Medical Association . 2018,第22期

机译：癌症相关基因癌症相关基因患者的突变检测肿瘤和正常DNA与基于指南的种系检测（Vol 318，PG 825,2017）
2. Mutation Detection in Patients With Advanced Cancer by Universal Sequencing of Cancer-Related Genes in Tumor and Normal DNA vs Guideline-Based Germline Testing [J] . Mandelker Diana, Zhang Liying, Kemel Yelena, JAMA: the Journal of the American Medical Association . 2017,第9期

机译：癌症相关基因的通用测序癌症和正常DNA癌症患者的突变检测与指南的种系检测
3. GERMLINE MUTATIONS IN CANCER PREDISPOSITION GENES IN A SUBSET OF PEDIATRIC ONCOLOGY PATIENTS UNDERGOING TARGETED SOLID TUMOR SEQUENCING USING MATCHED NORMAL DNA [J] . Walsh Michael, Neerav Shukla, Joseph V, Pediatric blood & cancer . 2016,第Suppla1期

机译：使用匹配的正常DNA对有针对性的固体肿瘤进行测序的小儿肿瘤患者亚群中癌症易感基因的生殖突变
4. Utility of ICE COLD-PCR Coupled to Sanger Sequencing or Next Generation Sequencing for Increased Mutation Detection Sensitivity During Patient Monitoring from Circulating Free DNA [C] . Katherine Richardson, Filip Janku, Ben Legendre, Molecular Medicine TRI-CON. . 2014

机译：冰冷PCR的效用偶联至Sanger测序或下一代测序，用于增加患者监测患者循环自由DNA期间的突变检测敏感性
5. Computational assessment of somatic missense mutations detected in tumor sequencing studies with cancer-specific high-throughput annotation of somatic mutations (CHASM). [D] . Carter, Hannah. 2012

机译：具有肿瘤特异性高通量体细胞突变（CHASM）的肿瘤测序研究中检测到的体细胞错义突变的计算评估。
6. Mutation Detection in Patients With Advanced Cancer by Universal Sequencing of Cancer-Related Genes in Tumor and Normal DNA vs Guideline-Based Germline Testing [O] . Diana Mandelker, Liying Zhang, Yelena Kemel, -1

机译：通过基于肿瘤和正常DNA的癌症相关基因的通用测序与基于指南的生殖细胞检测对突变的晚期癌症患者进行突变检测
7. Tumor mismatch repair immunohistochemistry and DNA MLH1 methylation testing of patients with endometrial cancer diagnosed at age younger than 60 years optimizes triage for population-level germline mismatch repair gene mutation testing [O] . Buchanan, D D, Tan, Y Y, Walsh, M D, 2014

机译：年龄小于60岁的子宫内膜癌患者的肿瘤错配修复免疫组织化学和DNA MLH1甲基化测试可优化人群水平种系错配修复基因突变测试的分类

Mutation Detection in Patients With Advanced Cancer by Universal Sequencing of Cancer-Related Genes in Tumor and Normal DNA vs Guideline-Based Germline Testing

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