scholarly journals Capture‐based next‐generation sequencing reveals multiple actionable mutations in cancer patients failed in traditional testing

2016 ◽  
Vol 4 (3) ◽  
pp. 262-272 ◽  
Author(s):  
Jing Xie ◽  
Xiongxiong Lu ◽  
Xue Wu ◽  
Xiaoyi Lin ◽  
Chao Zhang ◽  
...  
2019 ◽  
Vol 26 (1) ◽  
pp. 109-114 ◽  
Author(s):  
Panwen Tian ◽  
Xiangyang Cheng ◽  
Zhengyi Zhao ◽  
Yuzi Zhang ◽  
Celimuge Bao ◽  
...  

2015 ◽  
Vol 4 (11) ◽  
pp. e1030561 ◽  
Author(s):  
Miran Jang ◽  
Poh-Yin Yew ◽  
Kosei Hasegawa ◽  
Yuji Ikeda ◽  
Keiichi Fujiwara ◽  
...  

2014 ◽  
Vol 56 (2) ◽  
pp. 193-198 ◽  
Author(s):  
Magdalena Ratajska ◽  
Magdalena Krygier ◽  
Maciej Stukan ◽  
Alina Kuźniacka ◽  
Magdalena Koczkowska ◽  
...  

Author(s):  
Noah A. Brown ◽  
Kojo S.J. Elenitoba-Johnson

Genomic testing enables clinical management to be tailored to individual cancer patients based on the molecular alterations present within cancer cells. Genomic sequencing results can be applied to detect and classify cancer, predict prognosis, and target therapies. Next-generation sequencing has revolutionized the field of cancer genomics by enabling rapid and cost-effective sequencing of large portions of the genome. With this technology, precision oncology is quickly becoming a realized paradigm for managing the treatment of cancer patients. However, many challenges must be overcome to efficiently implement the transition of next-generation sequencing from research applications to routine clinical practice, including using specimens commonly available in the clinical setting; determining how to process, store, and manage large amounts of sequencing data; determining how to interpret and prioritize molecular findings; and coordinating health professionals from multiple disciplines.


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