Rita Guerreiro
A comprehensive assessment of benign genetic variability for neurodegenerative disorders
Guerreiro, Rita; Sassi, Celeste; Gibbs, Jesse; Edsall, Connor; Hernandez, Dena; Brown, Kristelle; Lupton, Michelle; Parkinnen, Laura; Ansorge, Olaf; Hodges, Angela; Ryten, Mina; Tienari, Pentti; Van Deerlin, Vivanna; Trojanowski, John; Morgan, Kevin; Powell, John; Singleton, Andrew; Hardy, John; Bras, Jose
Authors
Celeste Sassi
Jesse Gibbs
Connor Edsall
Dena Hernandez
Dr KRISTELLE BROWN KRISTELLE.BROWN@NOTTINGHAM.AC.UK
TEACHING ASSOCIATE
Michelle Lupton
Laura Parkinnen
Olaf Ansorge
Angela Hodges
Mina Ryten
Pentti Tienari
Vivanna Van Deerlin
John Trojanowski
Kevin Morgan
John Powell
Andrew Singleton
John Hardy
Jose Bras
Abstract
Over the last few years, as more and more sequencing studies have been performed, it has become apparent that the identification of pathogenic mutations is, more often than not, a complex issue. Here, with a focus on neurodegenerative diseases, we have performed a survey of coding genetic variability that is unlikely to be pathogenic. We have performed whole-exome sequencing in 478 samples derived from several brain banks in the United Kingdom and the United States of America. Samples were included when subjects were, at death, over 60 years of age, had no signs of neurological disease and were subjected to a neuropathological examination, which revealed no evidence of neurodegeneration. This information will be valuable to studies of genetic variability as a causal factor for neurodegenerative syndromes. We envisage it will be particularly relevant for diagnostic laboratories as a filter step to the results being produced by either genome-wide or gene-panel sequencing. We have made this data publicly available at www.alzforum.org/exomes/hex.
Citation
Guerreiro, R., Sassi, C., Gibbs, J., Edsall, C., Hernandez, D., Brown, K., Lupton, M., Parkinnen, L., Ansorge, O., Hodges, A., Ryten, M., Tienari, P., Van Deerlin, V., Trojanowski, J., Morgan, K., Powell, J., Singleton, A., Hardy, J., & Bras, J. (2018). A comprehensive assessment of benign genetic variability for neurodegenerative disorders. https://doi.org/10.1101/270686
Journal Article Type | Article |
---|---|
Acceptance Date | Feb 23, 2018 |
Publication Date | Feb 23, 2018 |
Deposit Date | Mar 22, 2018 |
Publicly Available Date | Mar 22, 2018 |
Journal | BioRxiv |
Peer Reviewed | Not Peer Reviewed |
Book Title | A comprehensive assessment of benign genetic variability for neurodegenerative disorders |
DOI | https://doi.org/10.1101/270686 |
Public URL | https://nottingham-repository.worktribe.com/output/916239 |
Publisher URL | https://doi.org/10.1101/270686 |
Contract Date | Mar 22, 2018 |
Files
270686.full.pdf
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Copyright Statement
Copyright information regarding this work can be found at the following address: http://creativecommons.org/licenses/by/4.0
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