Correction: Long-read trio sequencing of individuals with unsolved intellectual disability

被引:0
|
作者
Marc Pauper
Erdi Kucuk
Aaron M. Wenger
Shreyasee Chakraborty
Primo Baybayan
Michael Kwint
Bart van der Sanden
Marcel R. Nelen
Ronny Derks
Han G. Brunner
Alexander Hoischen
Lisenka E. L. M. Vissers
Christian Gilissen
机构
[1] Radboud University Medical Center,Department of Human Genetics
[2] Radboud Institute for Molecular Life Sciences,Donders Institute for Brain, Cognition and Behaviour
[3] Radboud University,Department of Clinical Genetics
[4] Pacific Biosciences,Department of Internal Medicine, Center for Infectious Diseases (RCI)
[5] Radboud University,undefined
[6] Maastricht University Medical Center,undefined
[7] Radboud University Medical Center,undefined
来源
关键词
D O I
暂无
中图分类号
学科分类号
摘要
A Correction to this paper has been published: https://doi.org/10.1038/s41431-021-00868-z
引用
收藏
页码:720 / 720
相关论文
共 50 条
  • [1] Long-read trio sequencing of individuals with unsolved intellectual disability
    Marc Pauper
    Erdi Kucuk
    Aaron M. Wenger
    Shreyasee Chakraborty
    Primo Baybayan
    Michael Kwint
    Bart van der Sanden
    Marcel R. Nelen
    Ronny Derks
    Han G. Brunner
    Alexander Hoischen
    Lisenka E. L. M. Vissers
    Christian Gilissen
    European Journal of Human Genetics, 2021, 29 : 637 - 648
  • [2] Long-read trio sequencing of individuals with unsolved intellectual disability
    Pauper, Marc
    Kucuk, Erdi
    Wenger, Aaron M.
    Chakraborty, Shreyasee
    Baybayan, Primo
    Kwint, Michael
    van der Sanden, Bart
    Nelen, Marcel R.
    Derks, Ronny
    Brunner, Han G.
    Hoischen, Alexander
    Vissers, Lisenka E. L. M.
    Gilissen, Christian
    EUROPEAN JOURNAL OF HUMAN GENETICS, 2021, 29 (04) : 637 - 648
  • [3] Clinical application of long-read sequencing in unsolved rare disease
    Farrow, Emily
    Miller, Neil
    Thiffault, Isabelle
    Baybayan, Primo
    Chakraborty, Shreyasee
    Lambert, Christine
    Rowell, William
    Wenger, Aaron
    Larrea, Andres
    Pastinen, Tomi
    MOLECULAR GENETICS AND METABOLISM, 2021, 132 : S215 - S216
  • [4] High-coverage, long-read sequencing of Han Chinese trio reference samples
    Ying-Chih Wang
    Nathan D. Olson
    Gintaras Deikus
    Hardik Shah
    Aaron M. Wenger
    Jonathan Trow
    Chunlin Xiao
    Stephen Sherry
    Marc L. Salit
    Justin M. Zook
    Melissa Smith
    Robert Sebra
    Scientific Data, 6
  • [5] High-coverage, long-read sequencing of Han Chinese trio reference samples
    Wang, Ying-Chih
    Olson, Nathan D.
    Deikus, Gintaras
    Shah, Hardik
    Wenger, Aaron M.
    Trow, Jonathan
    Xiao, Chunlin
    Sherry, Stephen
    Salit, Marc L.
    Zook, Justin M.
    Smith, Melissa
    Sebra, Robert
    SCIENTIFIC DATA, 2019, 6 (1)
  • [6] Genome sequencing using long-read sequencing
    McEwen, Juan Guillermo
    Gomez, Oscar Mauricio
    REVISTA DE LA ACADEMIA COLOMBIANA DE CIENCIAS EXACTAS FISICAS Y NATURALES, 2023, 47 (183): : 439 - 444
  • [7] Targeted long-read sequencing identifies missing pathogenic variants in unsolved Werner syndrome cases
    Miller, Danny E.
    Lee, Lin
    Galey, Miranda
    Kandhaya-Pillai, Renuka
    Tischkowitz, Marc
    Amalnath, Deepak
    Vithlani, Avadh
    Yokote, Koutaro
    Kato, Hisaya
    Maezawa, Yoshiro
    Takada-Watanabe, Aki
    Takemoto, Minoru
    Martin, George M.
    Eichler, Evan E.
    Hisama, Fuki M.
    Oshima, Junko
    JOURNAL OF MEDICAL GENETICS, 2022, 59 (11) : 1087 - 1094
  • [8] Targeted long-read sequencing identifies missing pathogenic variant in unsolved 11β-hydroxylase deficiency
    Liu, Jidong
    Tian, Huihui
    Jin, Xinchen
    Wang, Yanxiang
    Zhang, Zhenhong
    Li, Mengxue
    Dai, Lulu
    Zhang, Xiaoli
    Jiang, Ling
    BMC ENDOCRINE DISORDERS, 2024, 24 (01)
  • [9] Long-read sequencing reveals chromothripsis in a molecularly unsolved case of Cornelia de Lange syndrome
    Bestetti, Ilaria
    Crippa, Milena
    Sironi, Alessandra
    Bellini, Matteo
    Tumiatti, Francesca
    Ballabio, Sara
    Ceriotti, Ferruccio
    Memo, Luigi
    Iascone, Maria
    Larizza, Lidia
    Finelli, Palma
    FRONTIERS IN GENETICS, 2024, 15
  • [10] Genomics in the long-read sequencing era
    van Dijk, Erwin L.
    Naquin, Delphine
    Gorrichon, Kevin
    Jaszczyszyn, Yan
    Ouazahrou, Rania
    Thermes, Claude
    Hernandez, Celine
    TRENDS IN GENETICS, 2023, 39 (09) : 649 - 671