<p>Forome Anfisa – an open source variant interpretation tool</p>

Michael Bouzinier; Serhey Trifonov; Joel Krier; Dmitry  Etin; Dimitri Olchanyi; Alexey Kargalov; Arezou Ghazani; Shamil Sunyaev

doi:10.7490/f1000research.1117292.1

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Bouzinier M, Trifonov S, Krier J et al. Forome Anfisa – an open source variant interpretation tool [version 1; not peer reviewed]. F1000Research 2019, 8(ISCB Comm J):1370 (slides) (https://doi.org/10.7490/f1000research.1117292.1)

NOTE: it is important to ensure the information in square brackets after the title is included in this citation.

Forome Anfisa – an open source variant interpretation tool

Michael Bouzinier¹, Serhey Trifonov, Joel Krier, Dmitry Etin², Dimitri Olchanyi, Alexey Kargalov, Arezou Ghazani, Shamil Sunyaev

Published 07 Aug 2019 (https://doi.org/10.7490/f1000research.1117292.1)

Author Affiliations

¹ Brigham and Women's Hospital, USA
² Forome Association, Austria

Copyright © 2019 Bouzinier M 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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Published 07 Aug 2019

Forome Anfisa – an open source variant interpretation tool
[version 1; not peer reviewed]

Michael Bouzinier¹, Serhey Trifonov, Joel Krier, Dmitry Etin², Dimitri Olchanyi, Alexey Kargalov, Arezou Ghazani, Shamil Sunyaev

Author Affiliations

¹ Brigham and Women's Hospital, USA
² Forome Association, Austria

Presented at

ISMB/ECCB 2019

Abstract

Competing Interests

No competing interests were disclosed

Keywords

Variant annotation, variant interpretation, integrated clinical research, whole genome sequencing, whole exome sequencing, crowdsourcing, collaboration

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