Novel Non-Coding, Coding and Structural Variants in Hairy Cell Leukemia from Whole Genome Transcriptome Sequencing

被引:1
|
作者
Blombery, Piers [1 ,2 ,3 ]
Walter, Wencke [4 ]
Hutter, Stephan [4 ]
Baer, Constance [4 ]
Sakuma, Maki [4 ]
Mueller, Heiko [4 ]
Wu, Simon [3 ]
Caldwell, Imogen R. [3 ]
Kern, Wolfgang [4 ]
Meggendorfer, Manja [4 ]
Haferlach, Claudia [4 ]
Haferlach, Torsten [4 ]
机构
[1] Torsten Haferlach Leukaemiediagnost Stiftung, Munich, Germany
[2] Univ Melbourne, Melbourne, Vic, Australia
[3] Peter MacCallum Canc Ctr, Melbourne, Vic, Australia
[4] MLL Munich Leukemia Lab, Munich, Germany
关键词
D O I
10.1182/blood-2022-163300
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
引用
收藏
页码:3546 / 3547
页数:2
相关论文
共 50 条
  • [31] Whole genome mutational landscape and characterization of non-coding and structural mutations in liver cancer
    Fujimoto, Akihiro
    Furuta, Mayuko
    Totoki, Yasushi
    Tsunoda, Tatsuhiko
    Kato, Mamoru
    Hiroki, Yamaue
    Kazuaki, Chayama
    Miyano, Satoru
    Aburatani, Hiroyuki
    Shibata, Tatsuhiro
    Nakagawa, Hidewaki
    GENES & GENETIC SYSTEMS, 2016, 91 (06) : 373 - 373
  • [32] Long non-coding RNAs and genome structural organisation
    Farabella, I.
    Di Stefano, M.
    Martin-Renom, M.
    FEBS JOURNAL, 2017, 284 : 319 - 319
  • [33] Towards better interpretation of variants in non-coding regions of the genome
    Whiffin, Nicola
    EUROPEAN JOURNAL OF HUMAN GENETICS, 2022, 30 (SUPPL 1) : 20 - 20
  • [34] Recommendations for clinical interpretation of variants in non-coding regions of the genome
    Ellingford, Jamie
    Ahn, Joo Wook
    Bagnall, Richard
    Baralle, Diana
    Barton, Stephanie
    Campbell, Christopher
    Downes, Kate
    Ellard, Sian
    Duff-Farrier, Celia
    FitzPatrick, David
    Greally, John
    Ingles, Jodie
    Krishnan, Neesha
    Lord, Jenny
    Martin, Hilary
    Newman, William
    O'Donnell-Luria, Anne
    Ramsden, Simon
    Rehm, Heidi
    Richardson, Ebony
    Singer-Berk, Moriel
    Taylor, Jenny
    Williams, Maggie
    Wood, Jordan
    Wright, Caroline
    Harrison, Steven
    Whiffin, Nicola
    EUROPEAN JOURNAL OF HUMAN GENETICS, 2023, 31 : 284 - 285
  • [35] Whole Genome Sequencing in Idiopathic and Familial Pulmonary Arterial Hypertension Reveals Causal Rare Coding and Non-coding Sequence Variation
    Graf, Stefan
    Bleda, Marta
    Haddinapola, Charaka
    Haimel, Matthias
    Bogaard, Harm J.
    Coglan, Gerry
    Corris, Paul A.
    Gibbs, J. S.
    Humbert, Marc
    Kiely, David G.
    Laurie, Allan
    Machado, Rajiv D.
    Peacock, Andrew J.
    Pepke-Zaba, Joanna
    Toshner, Mark
    Trembath, Richard C.
    Noordegraaf, Anton Vonk
    Wharton, John
    Wilkins, Martin
    Wort, Stephen J.
    Morrell, Nicholas W.
    CIRCULATION, 2016, 134
  • [36] Deep sequencing of small RNA transcriptome reveals novel non-coding RNAs in hepatocellular carcinoma
    Law, Priscilla T. -Y.
    Qin, Hao
    Ching, Arthur K. -K.
    Lai, Keng Po
    Co, Ngai Na
    He, Mian
    Lung, Raymond W. -M.
    Chan, Anthony W. -H.
    Chan, Ting-Fung
    Wong, Nathalie
    JOURNAL OF HEPATOLOGY, 2013, 58 (06) : 1165 - 1173
  • [37] Non-coding RNAs: A novel level of genome complexity
    Irminger-Finger, Irmgard
    Kargul, Joanna
    Laurent, Geoff J.
    INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY, 2014, 54 : 286 - 286
  • [38] HCV infection, IFN response and the coding and non-coding host cell genome
    Carnero, Elena
    Fortes, Puri
    VIRUS RESEARCH, 2016, 212 : 85 - 102
  • [39] Multidisciplinary team directed analysis of whole genome sequencing reveals pathogenic non-coding variants in molecularly undiagnosed inherited retinal dystrophies
    Varela, Malena Daich
    Bellingham, James
    Motta, Fabiana
    Jurkute, Neringa
    Ellingford, Jamie M.
    Quinodoz, Mathieu
    Oprych, Kathryn
    Niblock, Michael
    Janeschitz-Kriegl, Lucas
    Kaminska, Karolina
    Cancellieri, Francesca
    Scholl, Hendrik P. N.
    Lenassi, Eva
    Schiff, Elena
    Knight, Hannah
    Black, Graeme
    Rivolta, Carlo
    Cheetham, Michael E.
    Michaelides, Michel
    Mahroo, Omar A.
    Moore, Anthony T.
    Webster, Andrew R.
    Arno, Gavin
    HUMAN MOLECULAR GENETICS, 2023, 32 (04) : 595 - 607
  • [40] GeneCaRNA: A gene-centric non-coding RNA compendium for disease decipherment by whole genome sequencing
    Aggarwal, Shalini
    Barshir, Ruth
    Fishilevich, Simon
    Rosenblum, Chana
    Iny-Stein, Tsippi
    Zelig, Ofer
    Guan-Golan, Yaron
    Safran, Marilyn
    Pietrokovski, Shmuel
    Lancet, Doron
    EUROPEAN JOURNAL OF HUMAN GENETICS, 2024, 32 : 300 - 301