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Original research
Nanopore sequencing as a scalable, cost-effective platform for analyzing polyclonal vector integration sites following clinical T cell therapy

Authors

  • Ping Zhang Department of Immunology, QIMR Berghofer Medical Research Institute, Herston, Queensland, Australia PubMed articlesGoogle scholar articles
  • Devika Ganesamoorthy Institute for Molecular Bioscience, University of Queensland, Brisbane, Queensland, Australia PubMed articlesGoogle scholar articles
  • Son Hoang Nguyen Institute for Molecular Bioscience, University of Queensland, Brisbane, Queensland, Australia PubMed articlesGoogle scholar articles
  • Raymond Au Department of Immunology, QIMR Berghofer Medical Research Institute, Herston, Queensland, Australia PubMed articlesGoogle scholar articles
  • Lachlan J Coin Institute for Molecular Bioscience, University of Queensland, Brisbane, Queensland, Australia Department of Clinical Pathology, The University of Melbourne, Melbourne, Victoria, Australia Department of Infectious Disease, Imperial College London, London, London, UK PubMed articlesGoogle scholar articles
  • Siok-Keen Tey Department of Immunology, QIMR Berghofer Medical Research Institute, Herston, Queensland, Australia Department of Haematology and Bone Marrow Transplantation, Royal Brisbane and Women's Hospital, Herston, Queensland, Australia Faculty of Medicine, University of Queensland, Brisbane, Queensland, Australia PubMed articlesGoogle scholar articles
  1. Correspondence to Siok-Keen Tey; siok.tey{at}qimrberghofer.edu.au
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Citation

Zhang P, Ganesamoorthy D, Nguyen SH, et al
Nanopore sequencing as a scalable, cost-effective platform for analyzing polyclonal vector integration sites following clinical T cell therapy

Publication history

  • Accepted March 28, 2020
  • First published June 10, 2020.
Online issue publication 
January 11, 2022

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