<p>Utanos: A general-purpose shallow whole genome sequencing analysis toolkit identifies interpretable copy number signatures in endometrial cancer</p>

J. Maxwell Douglas; Branden J. Lynch; Nirupama Tamvada; David G. Huntsman; Yongjin Park

doi:10.7490/f1000research.1120070.1

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Douglas JM, Lynch BJ, Tamvada N et al. Utanos: A general-purpose shallow whole genome sequencing analysis toolkit identifies interpretable copy number signatures in endometrial cancer [version 1; not peer reviewed]. F1000Research 2025, 14:1 (poster) (https://doi.org/10.7490/f1000research.1120070.1)

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Utanos: A general-purpose shallow whole genome sequencing analysis toolkit identifies interpretable copy number signatures in endometrial cancer

J. Maxwell Douglas, Branden J. Lynch, Nirupama Tamvada, David G. Huntsman, Yongjin Park¹

Published 01 Jan 2025 (https://doi.org/10.7490/f1000research.1120070.1)

Author Affiliations

¹ Department of Molecular Oncology, BC Cancer Research Center, Vancouver, BC, Canada

Copyright © 2025 Douglas JM 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 01 Jan 2025

Utanos: A general-purpose shallow whole genome sequencing analysis toolkit identifies interpretable copy number signatures in endometrial cancer
[version 1; not peer reviewed]

J. Maxwell Douglas, Branden J. Lynch, Nirupama Tamvada, David G. Huntsman, Yongjin Park¹

Author Affiliations

¹ Department of Molecular Oncology, BC Cancer Research Center, Vancouver, BC, Canada

Presented at

Intelligent Systems for Molecular Biology Conference (ISMB), 2025

Abstract

Competing Interests

No competing interests were disclosed

Keywords

Shallow whole-genome sequencing, genomics, endometrial cancer, non-negative matrix factorization

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