<p>Identification of epimutations in rare diseases from a single patient perspective</p>

Robin Grolaux; Alexis Hardy; Matthieu Defrance

doi:10.7490/f1000research.1119193.1

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Grolaux R, Hardy A and Defrance M. Identification of epimutations in rare diseases from a single patient perspective [version 1; not peer reviewed]. F1000Research 2022, 11:1319 (poster) (https://doi.org/10.7490/f1000research.1119193.1)

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Identification of epimutations in rare diseases from a single patient perspective

Robin Grolaux, Alexis Hardy, Matthieu Defrance¹

Published 15 Nov 2022 (https://doi.org/10.7490/f1000research.1119193.1)

Author Affiliations

¹ Univeristy Libre de Bruxelles, Belgium

Copyright © 2022 Grolaux R et al. This is an open access work distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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CITE

Published 15 Nov 2022

Identification of epimutations in rare diseases from a single patient perspective
[version 1; not peer reviewed]

Robin Grolaux, Alexis Hardy, Matthieu Defrance¹

Author Affiliations

¹ Univeristy Libre de Bruxelles, Belgium

Presented at

European Conference on Computational Biology (ECCB) 2022

Abstract

Competing Interests

No competing interests were disclosed

Keywords

DNA methylation, differentially methylated regions, rare diseases, Beckwith-Wiedemann syndrome, imprinting, statistical method

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