Toward best practice in cancer mutation detection with whole-genome and whole-exome sequencing-Reference-Cited by-同舟云学术

Toward best practice in cancer mutation detection with whole-genome and whole-exome sequencing

Published:2021-09 Issue:9 Volume:39 Page:1141-1150
ISSN:1087-0156
Container-title:Nature Biotechnology
language:en
Short-container-title:Nat Biotechnol

Author:

Xiao Wenming^ORCID,Ren Luyao,Chen Zhong^ORCID,Fang Li Tai^ORCID,Zhao Yongmei^ORCID,Lack Justin,Guan Meijian,Zhu Bin^ORCID,Jaeger Erich,Kerrigan Liz,Blomquist Thomas M.,Hung Tiffany,Sultan Marc,Idler Kenneth,Lu Charles,Scherer Andreas^ORCID,Kusko Rebecca^ORCID,Moos Malcolm,Xiao Chunlin^ORCID,Sherry Stephen T.,Abaan Ogan D.,Chen Wanqiu^ORCID,Chen Xin,Nordlund Jessica,Liljedahl Ulrika,Maestro Roberta^ORCID,Polano Maurizio,Drabek Jiri,Vojta Petr^ORCID,Kõks Sulev^ORCID,Reimann Ene^ORCID,Madala Bindu Swapna,Mercer Timothy^ORCID,Miller Chris,Jacob Howard,Truong Tiffany,Moshrefi Ali,Natarajan Aparna,Granat Ana,Schroth Gary P.^ORCID,Kalamegham Rasika,Peters Eric,Petitjean Virginie,Walton Ashley,Shen Tsai-Wei^ORCID,Talsania Keyur,Vera Cristobal Juan,Langenbach Kurt,de Mars Maryellen,Hipp Jennifer A.,Willey James C.,Wang Jing,Shetty Jyoti,Kriga Yuliya,Raziuddin Arati^ORCID,Tran Bao,Zheng Yuanting,Yu Ying,Cam Margaret,Jailwala Parthav,Nguyen Cu,Meerzaman Daoud,Chen Qingrong,Yan Chunhua,Ernest Ben,Mehra Urvashi,Jensen Roderick V.,Jones Wendell^ORCID,Li Jian-Liang^ORCID,Papas Brian N.,Pirooznia Mehdi^ORCID,Chen Yun-Ching,Seifuddin Fayaz^ORCID,Li Zhipan,Liu Xuelu,Resch Wolfgang,Wang Jingya,Wu Leihong,Yavas Gokhan,Miles Corey,Ning Baitang,Tong Weida,Mason Christopher E.^ORCID,Donaldson Eric,Lababidi Samir,Staudt Louis M.,Tezak Zivana,Hong Huixiao^ORCID,Wang Charles^ORCID,Shi Leming^ORCID

Publisher

Springer Science and Business Media LLC

Subject

Biomedical Engineering,Molecular Medicine,Applied Microbiology and Biotechnology,Bioengineering,Biotechnology

Link

https://www.nature.com/articles/s41587-021-00994-5.pdf

Reference51 articles.

1. Glasziou, P., Meats, E., Heneghan, C. & Shepperd, S. What is missing from descriptions of treatment in trials and reviews? Brit. Med. J. 336, 1472–1474 (2008).

2. Vasilevsky, N. A. et al. On the reproducibility of science: unique identification of research resources in the biomedical literature. PeerJ 1, e148 (2013).

3. Begley, C. G. & Ellis, L. M. Drug development: raise standards for preclinical cancer research. Nature 483, 531–533 (2012).

4. Alioto, T. S. et al. A comprehensive assessment of somatic mutation detection in cancer using whole-genome sequencing. Nat. Commun. 6, 10001 (2015).

5. Griffith, M. et al. Genome Modeling System: a knowledge management platform for genomics. PLoS Comput. Biol. 11, e1004274 (2015).

Cited by 93 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Validation and Implementation of a Somatic-Only Tumor Exome for Routine Clinical Application;The Journal of Molecular Diagnostics;2024-09

2. Benchmarking Whole Exome Sequencing in the German Network for Personalized Medicine;European Journal of Cancer;2024-09

3. Genomic Insights into Idiopathic Granulomatous Mastitis through Whole-Exome Sequencing: A Case Report of Eight Patients;International Journal of Molecular Sciences;2024-08-21

4. Chinese expert consensus on standard technical specifications for a gut microecomics laboratory (Review);Experimental and Therapeutic Medicine;2024-08-20

5. GENOMICON-Seq: A comprehensive tool for the simulation of mutations in amplicon and whole exome sequencing;2024-08-17