Cargando…

Functional Assessment of Genetic Variants with Outcomes Adapted to Clinical Decision-Making

Understanding the medical effect of an ever-growing number of human variants detected is a long term challenge in genetic counseling. Functional assays, based on in vitro or in vivo evaluations of the variant effects, provide essential information, but they require robust statistical validation, as...

Descripción completa

Detalles Bibliográficos
Autores principales: Thouvenot, Pierre, Ben Yamin, Barbara, Fourrière, Lou, Lescure, Aurianne, Boudier, Thomas, Del Nery, Elaine, Chauchereau, Anne, Goldgar, David E., Houdayer, Claude, Stoppa-Lyonnet, Dominique, Nicolas, Alain, Millot, Gaël A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4894565/
https://www.ncbi.nlm.nih.gov/pubmed/27272900
http://dx.doi.org/10.1371/journal.pgen.1006096
_version_ 1782435687088259072
author Thouvenot, Pierre
Ben Yamin, Barbara
Fourrière, Lou
Lescure, Aurianne
Boudier, Thomas
Del Nery, Elaine
Chauchereau, Anne
Goldgar, David E.
Houdayer, Claude
Stoppa-Lyonnet, Dominique
Nicolas, Alain
Millot, Gaël A.
author_facet Thouvenot, Pierre
Ben Yamin, Barbara
Fourrière, Lou
Lescure, Aurianne
Boudier, Thomas
Del Nery, Elaine
Chauchereau, Anne
Goldgar, David E.
Houdayer, Claude
Stoppa-Lyonnet, Dominique
Nicolas, Alain
Millot, Gaël A.
author_sort Thouvenot, Pierre
collection PubMed
description Understanding the medical effect of an ever-growing number of human variants detected is a long term challenge in genetic counseling. Functional assays, based on in vitro or in vivo evaluations of the variant effects, provide essential information, but they require robust statistical validation, as well as adapted outputs, to be implemented in the clinical decision-making process. Here, we assessed 25 pathogenic and 15 neutral missense variants of the BRCA1 breast/ovarian cancer susceptibility gene in four BRCA1 functional assays. Next, we developed a novel approach that refines the variant ranking in these functional assays. Lastly, we developed a computational system that provides a probabilistic classification of variants, adapted to clinical interpretation. Using this system, the best functional assay exhibits a variant classification accuracy estimated at 93%. Additional theoretical simulations highlight the benefit of this ready-to-use system in the classification of variants after functional assessment, which should facilitate the consideration of functional evidences in the decision-making process after genetic testing. Finally, we demonstrate the versatility of the system with the classification of siRNAs tested for human cell growth inhibition in high throughput screening.
format Online
Article
Text
id pubmed-4894565
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-48945652016-06-23 Functional Assessment of Genetic Variants with Outcomes Adapted to Clinical Decision-Making Thouvenot, Pierre Ben Yamin, Barbara Fourrière, Lou Lescure, Aurianne Boudier, Thomas Del Nery, Elaine Chauchereau, Anne Goldgar, David E. Houdayer, Claude Stoppa-Lyonnet, Dominique Nicolas, Alain Millot, Gaël A. PLoS Genet Research Article Understanding the medical effect of an ever-growing number of human variants detected is a long term challenge in genetic counseling. Functional assays, based on in vitro or in vivo evaluations of the variant effects, provide essential information, but they require robust statistical validation, as well as adapted outputs, to be implemented in the clinical decision-making process. Here, we assessed 25 pathogenic and 15 neutral missense variants of the BRCA1 breast/ovarian cancer susceptibility gene in four BRCA1 functional assays. Next, we developed a novel approach that refines the variant ranking in these functional assays. Lastly, we developed a computational system that provides a probabilistic classification of variants, adapted to clinical interpretation. Using this system, the best functional assay exhibits a variant classification accuracy estimated at 93%. Additional theoretical simulations highlight the benefit of this ready-to-use system in the classification of variants after functional assessment, which should facilitate the consideration of functional evidences in the decision-making process after genetic testing. Finally, we demonstrate the versatility of the system with the classification of siRNAs tested for human cell growth inhibition in high throughput screening. Public Library of Science 2016-06-06 /pmc/articles/PMC4894565/ /pubmed/27272900 http://dx.doi.org/10.1371/journal.pgen.1006096 Text en © 2016 Thouvenot et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Thouvenot, Pierre
Ben Yamin, Barbara
Fourrière, Lou
Lescure, Aurianne
Boudier, Thomas
Del Nery, Elaine
Chauchereau, Anne
Goldgar, David E.
Houdayer, Claude
Stoppa-Lyonnet, Dominique
Nicolas, Alain
Millot, Gaël A.
Functional Assessment of Genetic Variants with Outcomes Adapted to Clinical Decision-Making
title Functional Assessment of Genetic Variants with Outcomes Adapted to Clinical Decision-Making
title_full Functional Assessment of Genetic Variants with Outcomes Adapted to Clinical Decision-Making
title_fullStr Functional Assessment of Genetic Variants with Outcomes Adapted to Clinical Decision-Making
title_full_unstemmed Functional Assessment of Genetic Variants with Outcomes Adapted to Clinical Decision-Making
title_short Functional Assessment of Genetic Variants with Outcomes Adapted to Clinical Decision-Making
title_sort functional assessment of genetic variants with outcomes adapted to clinical decision-making
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4894565/
https://www.ncbi.nlm.nih.gov/pubmed/27272900
http://dx.doi.org/10.1371/journal.pgen.1006096
work_keys_str_mv AT thouvenotpierre functionalassessmentofgeneticvariantswithoutcomesadaptedtoclinicaldecisionmaking
AT benyaminbarbara functionalassessmentofgeneticvariantswithoutcomesadaptedtoclinicaldecisionmaking
AT fourrierelou functionalassessmentofgeneticvariantswithoutcomesadaptedtoclinicaldecisionmaking
AT lescureaurianne functionalassessmentofgeneticvariantswithoutcomesadaptedtoclinicaldecisionmaking
AT boudierthomas functionalassessmentofgeneticvariantswithoutcomesadaptedtoclinicaldecisionmaking
AT delneryelaine functionalassessmentofgeneticvariantswithoutcomesadaptedtoclinicaldecisionmaking
AT chauchereauanne functionalassessmentofgeneticvariantswithoutcomesadaptedtoclinicaldecisionmaking
AT goldgardavide functionalassessmentofgeneticvariantswithoutcomesadaptedtoclinicaldecisionmaking
AT houdayerclaude functionalassessmentofgeneticvariantswithoutcomesadaptedtoclinicaldecisionmaking
AT stoppalyonnetdominique functionalassessmentofgeneticvariantswithoutcomesadaptedtoclinicaldecisionmaking
AT nicolasalain functionalassessmentofgeneticvariantswithoutcomesadaptedtoclinicaldecisionmaking
AT millotgaela functionalassessmentofgeneticvariantswithoutcomesadaptedtoclinicaldecisionmaking