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

James Dominic Mills; Sanjay M Sisodiya

doi:10.1093/braincomms/fcab280

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

Brain Commun. 2021 Nov 19;3(4):fcab280. doi: 10.1093/braincomms/fcab280. eCollection 2021.

Authors

James Dominic Mills^{1

2

3}, Sanjay M Sisodiya^{1

2}

Affiliations

¹ Department of Clinical and Experimental Epilepsy, UCL Queen Square Institute of Neurology, London, UK.
² Chalfont Centre for Epilepsy, Buckinghamshire, UK.
³ Department of (Neuro)Pathology, Amsterdam UMC, University of Amsterdam, Amsterdam Neuroscience, Amsterdam, The Netherlands.

Abstract

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).