Whole-genome sequencing: identification of additional pathogenic variation across the genome

This scientific commentary refers to ‘Genome sequencing identifies rare tandem repeat expansions and copy number variants in Lennox–Gastaut syndrome’, by Qaiser et al. (https://doi.org/10.1093/braincomms/fcab207).

Detalles Bibliográficos
Autores principales: Mills, James Dominic, Sisodiya, Sanjay M
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
Materias:
Scientific Commentary
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8634381/
https://www.ncbi.nlm.nih.gov/pubmed/34859220
http://dx.doi.org/10.1093/braincomms/fcab280
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author Mills, James Dominic
Sisodiya, Sanjay M
author_facet Mills, James Dominic
Sisodiya, Sanjay M
author_sort Mills, James Dominic
collection PubMed
description This scientific commentary refers to ‘Genome sequencing identifies rare tandem repeat expansions and copy number variants in Lennox–Gastaut syndrome’, by Qaiser et al. (https://doi.org/10.1093/braincomms/fcab207).
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spelling pubmed-86343812021-12-01 Whole-genome sequencing: identification of additional pathogenic variation across the genome Mills, James Dominic Sisodiya, Sanjay M Brain Commun Scientific Commentary This scientific commentary refers to ‘Genome sequencing identifies rare tandem repeat expansions and copy number variants in Lennox–Gastaut syndrome’, by Qaiser et al. (https://doi.org/10.1093/braincomms/fcab207). Oxford University Press 2021-11-19 /pmc/articles/PMC8634381/ /pubmed/34859220 http://dx.doi.org/10.1093/braincomms/fcab280 Text en © The Author(s) (2021). Published by Oxford University Press on behalf of the Guarantors of Brain. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Scientific Commentary
Mills, James Dominic
Sisodiya, Sanjay M
Whole-genome sequencing: identification of additional pathogenic variation across the genome
title Whole-genome sequencing: identification of additional pathogenic variation across the genome
title_full Whole-genome sequencing: identification of additional pathogenic variation across the genome
title_fullStr Whole-genome sequencing: identification of additional pathogenic variation across the genome
title_full_unstemmed Whole-genome sequencing: identification of additional pathogenic variation across the genome
title_short Whole-genome sequencing: identification of additional pathogenic variation across the genome
title_sort whole-genome sequencing: identification of additional pathogenic variation across the genome
topic Scientific Commentary
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8634381/
https://www.ncbi.nlm.nih.gov/pubmed/34859220
http://dx.doi.org/10.1093/braincomms/fcab280
work_keys_str_mv AT millsjamesdominic wholegenomesequencingidentificationofadditionalpathogenicvariationacrossthegenome
AT sisodiyasanjaym wholegenomesequencingidentificationofadditionalpathogenicvariationacrossthegenome

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