Copy Number Variants Identified By Shallow Whole-Genome Sequencing in Multiple Myeloma

被引：0
|
作者：
Li, Jiali [1 ]
Xiang, Xixi [1 ]
Rao, Jun [2 ]
Zhou, Sha [3 ]
Zeng, Yunjing [1 ]
Zhang, Xi [2 ]
Gao, Li [1 ]
机构：
[1] Army Med Univ, Xinqiao Hosp, Chongqing, Peoples R China
[2] Army Med Univ, Med Ctr Hematol, State Key Lab Trauma & Chem Poisoning, Chongqing Key Lab Hematol & Microenvironm,Xinqiao, Chongqing, Peoples R China
[3] Army Med Univ, Xinqiao Hosp, Dept Hematol, Chongqing, Peoples R China
来源：
BLOOD | 2024年 / 144卷
关键词：
D O I：
10.1182/blood-2024-206990
中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
引用
收藏
页码：6931 / 6931
页数：1
相关论文
共 50 条
  • [11] Genome-wide detection of copy number variants in European autochthonous and commercial pig breeds by whole-genome sequencing of DNA pools identified breed-characterising copy number states
    Bovo, S.
    Ribani, A.
    Munoz, M.
    Alves, E.
    Araujo, J. P.
    Bozzi, R.
    Charneca, R.
    Di Palma, F.
    Etherington, G.
    Fernandez, A., I
    Garcia, F.
    Garcia-Casco, J.
    Karolyi, D.
    Gallo, M.
    Gvozdanovic, K.
    Martins, J. M.
    Mercat, M. J.
    Nunez, Y.
    Quintanilla, R.
    Razmaite, V
    Riquet, J.
    Savic, R.
    Schiavo, G.
    Skrlep, M.
    Usai, G.
    Utzeri, V. J.
    Zimmer, C.
    Ovilo, C.
    Fontanesi, L.
    Radovie, C.
    ANIMAL GENETICS, 2020, 51 (04) : 541 - 556
  • [12] Clinical Validation of Whole-Genome Sequencing for the Detection of Copy Number Variation
    Thayanithy, V.
    Thyagarajan, B.
    Bower, M.
    Munro, S.
    Lam, H.
    Bray, S.
    Vivek, S.
    Schomaker, M.
    Daniel, J.
    Henzler, C.
    Nelson, A.
    Yohe, S.
    McIntyre, K.
    JOURNAL OF MOLECULAR DIAGNOSTICS, 2022, 24 (10): : S27 - S27
  • [13] Detecting Copy Number Variation from Whole-Genome Sequencing Data
    Jobanputra, V.
    Klein, R.
    Nahum, O.
    Yang, S.
    Ballinger, D.
    Beilharz, E.
    Levy, B.
    CYTOGENETIC AND GENOME RESEARCH, 2014, 142 (03)
  • [14] Pathogenic variants in KPTN gene identified by clinical whole-genome sequencing
    Thiffault, Isabelle
    Atherton, Andrea
    Heese, Bryce A.
    Abdelmoity, Ahmed T.
    Pawar, Kailash
    Farrow, Emily
    Zellmer, Lee
    Miller, Neil
    Soden, Sarah
    Saunders, Carol
    COLD SPRING HARBOR MOLECULAR CASE STUDIES, 2020, 6 (03):
  • [15] DETECTION OF UROTHELIAL CARCINOMA BASED ON COPY NUMBER PROFILES OF URINARY CFDNA USING SHALLOW WHOLE-GENOME SEQUENCING
    Gong, Yanqing
    Ge, Guangzhe
    Peng, Ding
    Guan, Bao
    Zhou, Yuanyuan
    Ci, Weimin
    Li, Xuesong
    Zhou, Liqun
    JOURNAL OF UROLOGY, 2020, 203 : E6 - E6
  • [16] Copy number variations identified using whole-genome sequencing as genetic markers for pediatrics patients with developmental defects
    Sun, Jiahong
    Huang, Chien-Ling
    Luk, Ho Ming
    Meng, Fei
    Lo, Fai Man
    Yip, Shea Ping
    EUROPEAN JOURNAL OF HUMAN GENETICS, 2023, 31 : 222 - 222
  • [17] Identification of Medium-Sized Copy Number Alterations in Whole-Genome Sequencing
    Ozer, Hatice Gulcin
    Usubalieva, Aisulu
    Dorrance, Adrienne
    Yilmaz, Ayse Selen
    Caligiuri, Michael
    Marcucci, Guido
    Huang, Kun
    CANCER INFORMATICS, 2014, 13 : 105 - 111
  • [18] Linked-read whole-genome sequencing resolves common and private structural variants in multiple myeloma
    Pena-Perez, Lucia
    Frengen, Nicolai
    Hauenstein, Julia
    Gran, Charlotte
    Gustafsson, Charlotte
    Eisfeldt, Jesper
    Kierczak, Marcin
    Taborsak-Lines, Fanny
    Olsen, Remi-Andre
    Wallblom, Ann
    Krstic, Aleksandra
    Ewels, Philip
    Lindstrand, Anna
    Mansson, Robert
    BLOOD ADVANCES, 2022, 6 (17) : 5009 - 5023
  • [19] Copy number alterations detected by whole-exome and whole-genome sequencing of esophageal adenocarcinoma
    Xiaoyu Wang
    Xiaohong Li
    Yichen Cheng
    Xin Sun
    Xibin Sun
    Steve Self
    Charles Kooperberg
    James Y. Dai
    Human Genomics, 9
  • [20] Tumor-associated copy number changes in the circulation of patients with prostate cancer identified through whole-genome sequencing
    Heitzer, Ellen
    Ulz, Peter
    Belic, Jelena
    Gutschi, Stefan
    Quehenberger, Franz
    Fischereder, Katja
    Benezeder, Theresa
    Auer, Martina
    Pischler, Carina
    Mannweiler, Sebastian
    Pichler, Martin
    Eisner, Florian
    Haeusler, Martin
    Riethdorf, Sabine
    Pantel, Klaus
    Samonigg, Hellmut
    Hoefler, Gerald
    Augustin, Herbert
    Geigl, Jochen B.
    Speicher, Michael R.
    GENOME MEDICINE, 2013, 5
12345