Recommendations for laboratory workflow that better support centralised amalgamation of genomic variant data: findings from CanVIG-UK national molecular laboratory survey

Allen, S. orcid.org/0000-0003-4928-2240, Loong, L., Garrett, A. orcid.org/0000-0001-8942-283X et al. (34 more authors) (2023) Recommendations for laboratory workflow that better support centralised amalgamation of genomic variant data: findings from CanVIG-UK national molecular laboratory survey. Journal of Medical Genetics. jmg-2023. ISSN 0022-2593

Abstract

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Copyright, Publisher and Additional Information: © Author(s) (or their employer(s)) 2023. Re-use permitted under CC BY. Published by BMJ. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed in accordance with the Creative Commons Attribution 4.0 Unported (CC BY 4.0) license, which permits others to copy, redistribute, remix, transform and build upon this work for any purpose, provided the original work is properly cited, a link to the licence is given, and indication of whether changes were made. See: https://creativecommons.org/licenses/by/4.0/.
Keywords: Clinical Laboratory Techniques; Genetic Testing; Genetics; Genomics; Molecular Diagnostic Techniques
Dates:
  • Accepted: 28 October 2023
  • Published (online): 22 December 2023
  • Published: December 2023
Institution: The University of Leeds
Depositing User: Symplectic Publications
Date Deposited: 07 Feb 2024 14:10
Last Modified: 07 Feb 2024 14:10
Published Version: http://dx.doi.org/10.1136/jmg-2023-109645
Status: Published
Publisher: BMJ
Identification Number: https://doi.org/10.1136/jmg-2023-109645
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