<p>A novel genetic region prioritization tool using a new statistical framework to analyse oligogenic diseases</p>

Simon Boutry; Raphaël Helaers; Tom Lenaerts; Miikka Vikkula

doi:10.7490/f1000research.1116109.1

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Boutry S, Helaers R, Lenaerts T and Vikkula M. A novel genetic region prioritization tool using a new statistical framework to analyse oligogenic diseases [version 1; not peer reviewed]. F1000Research 2018, 7:1496 (poster) (https://doi.org/10.7490/f1000research.1116109.1)

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A novel genetic region prioritization tool using a new statistical framework to analyse oligogenic diseases

Simon Boutry¹, Raphaël Helaers, Tom Lenaerts, Miikka Vikkula

Published 19 Sep 2018 (https://doi.org/10.7490/f1000research.1116109.1)

Author Affiliations

¹ de Duve Institute (Catholic University of Louvain), Belgium

Copyright © 2018 Boutry S 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 19 Sep 2018

A novel genetic region prioritization tool using a new statistical framework to analyse oligogenic diseases
[version 1; not peer reviewed]

Simon Boutry¹, Raphaël Helaers, Tom Lenaerts, Miikka Vikkula

Author Affiliations

¹ de Duve Institute (Catholic University of Louvain), Belgium

Presented at

Genome Informatics 2018

Abstract

Competing Interests

No competing interests were disclosed

Keywords

Oligogenic, rare variant, Burden, aggregation test, NGS, WES, WGS, prioritization tool

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