Copy number variation of urine exfoliated cells by low-coverage whole genome sequencing for diagnosis of prostate adenocarcinoma: a prospective cohort study

被引:0
|
作者
Youyan Guan
Xiaobing Wang
Kaopeng Guan
Dong Wang
Xingang Bi
Zhendong Xiao
Zejun Xiao
Xingli Shan
Linjun Hu
Jianhui Ma
Changling Li
Yong Zhang
Jianzhong Shou
Baiyun Wang
Ziliang Qian
Nianzeng Xing
机构
[1] Chinese Academy of Medical Sciences and Peking Union Medical College,Department of Urology, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital
[2] Chinese Academy of Medical Sciences and Peking Union Medical College,State Key Laboratory of Molecular Oncology, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital
[3] Cancer Hospital of Huanxing,undefined
[4] Hongyuan Biotech,undefined
[5] Biobay,undefined
来源
关键词
D O I
暂无
中图分类号
学科分类号
摘要
引用
收藏
相关论文
共 50 条
  • [21] Re: Noninvasive Detection of Urothelial Carcinoma by Cost-Effective Low-Coverage Whole-Genome Sequencing from Urine-Exfoliated Cell DNA
    不详
    JOURNAL OF UROLOGY, 2021, 206 (04): : 1061 - 1061
  • [22] Low-coverage genome sequencing is an efficient approach for the detection of clinically relevant copy-number variants and mtDNA variants
    Pajusalu, Sander
    Oja, Kaisa Teele
    Samarina, Ustina
    Tooming, Mikk
    Kahre, Tiina
    Ounap, Katrin
    EUROPEAN JOURNAL OF HUMAN GENETICS, 2023, 31 : 592 - 592
  • [23] Non-invasive detection of biliary tract cancer by low-coverage whole genome sequencing from plasma cell-free DNA: A prospective cohort study
    Wang, Xiang
    Fu, Xiao-Hui
    Qian, Zi-Liang
    Zhao, Teng
    Duan, An-Qi
    Ruan, Xiang
    Zhu, Bin
    Yin, Lei
    Zhang, Yong-Jie
    Yu, Wen-Long
    TRANSLATIONAL ONCOLOGY, 2021, 14 (01):
  • [24] Genome-wide copy number variation detection in a large cohort of diverse horse breeds by whole-genome sequencing
    Tang, Xiangwei
    Zhu, Bo
    Ren, Ruimin
    Chen, Bin
    Li, Sheng
    Gu, Jingjing
    FRONTIERS IN VETERINARY SCIENCE, 2023, 10
  • [25] Circulating tumor DNA (ctDNA) analysis by low-coverage whole genome sequencing (lcWGS) of resectable esophageal adenocarcinoma (rEAC) patients.
    van den Ende, Tom
    Creemers, Aafke
    van der Pol, Ymke
    Boers, Dries
    Henegouwen, Mark I. Van Berge
    Gisbertz, Suzanne S.
    Geijsen, E. Debby
    Hulshof, Maarten C. C. M.
    Dijk, Frederike
    van Grieken, Nicole C. T.
    Pegtel, D. Michiel
    Derks, Sarah
    Bijlsma, Maarten F.
    Mouliere, Florent
    Van Laarhoven, Hanneke W. M.
    JOURNAL OF CLINICAL ONCOLOGY, 2021, 39 (15)
  • [26] Whole Genome Low-Coverage Sequencing Concurrently Detecting Copy Number Variations and Their Underlying Complex Chromosomal Rearrangements by Systematic Breakpoint Mapping in Intellectual Deficiency/Developmental Delay Patients
    Xiao, Bing
    Ye, Xiantao
    Wang, Lili
    Fan, Yanjie
    Gu, Xuefan
    Ji, Xing
    Sun, Yu
    Yu, Yongguo
    FRONTIERS IN GENETICS, 2020, 11
  • [27] Low-Coverage Whole Genome Sequencing of Cell-Free DNA From Immunosuppressed Cancer Patients Enables Tumor Fraction Determination and Reveals Relevant Copy Number Alterations
    Bouzidi, Amira
    Labreche, Karim
    Baron, Marine
    Veyri, Marianne
    Denis, Jerome Alexandre
    Touat, Mehdi
    Sanson, Marc
    Davi, Frederic
    Guillerm, Erell
    Jouannet, Stephanie
    Charlotte, Frederic
    Bielle, Franck
    Choquet, Sylvain
    Boelle, Pierre-Yves
    Cadranel, Jacques
    Leblond, Veronique
    Autran, Brigitte
    Lacorte, Jean-Marc
    Spano, Jean-Philippe
    Coulet, Florence
    FRONTIERS IN CELL AND DEVELOPMENTAL BIOLOGY, 2021, 9
  • [28] Genomic analysis of Korean patients with advanced prostate cancer by use of a comprehensive next-generation sequencing panel and low-coverage, whole-genome sequencing
    Kang, Minyong
    Cho, Eunhae
    Jang, Jahyun
    Lee, Junnam
    Jeon, Youngjoo
    Jeong, Byong Chang
    Seo, Seong Il
    Jeon, Seong Soo
    Lee, Hyun Moo
    Choi, Han Yong
    Jeon, Hwang Gyun
    INVESTIGATIVE AND CLINICAL UROLOGY, 2019, 60 (04) : 227 - 234
  • [29] Evaluation of tools for identifying large copy number variations from ultra-low-coverage whole-genome sequencing data
    Johannes Smolander
    Sofia Khan
    Kalaimathy Singaravelu
    Leni Kauko
    Riikka J. Lund
    Asta Laiho
    Laura L. Elo
    BMC Genomics, 22
  • [30] Evaluation of tools for identifying large copy number variations from ultra-low-coverage whole-genome sequencing data
    Smolander, Johannes
    Khan, Sofia
    Singaravelu, Kalaimathy
    Kauko, Leni
    Lund, Riikka J.
    Laiho, Asta
    Elo, Laura L.
    BMC GENOMICS, 2021, 22 (01)