HAT: De novo variant calling for highly accurate short-read and long-read sequencing data

Authors

Jeffrey K Ng, Washington University School of Medicine in St. Louis
Tychele N Turner, Washington University School of Medicine in St. Louis

Journal

Bioinformatics

Publication Date

1-2-2024

Volume

40

Issue

1

First Page

btad775

Document Type

Open Access Publication

DOI

10.1093/bioinformatics/btad775

Rights and Permissions

Jeffrey K Ng, Tychele N Turner, HAT: de novo variant calling for highly accurate short-read and long-read sequencing data, Bioinformatics, Volume 40, Issue 1, January 2024, btad775, https://doi.org/10.1093/bioinformatics/btad775. https://academic.oup.com/bioinformatics/article/40/1/btad775/7510834?login=true. © The Author(s) 2024. Published by Oxford University Press. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.

Recommended Citation

Ng, Jeffrey K and Turner, Tychele N, "HAT: De novo variant calling for highly accurate short-read and long-read sequencing data." Bioinformatics. 40, 1. btad775 (2024).
https://digitalcommons.wustl.edu/oa_4/2893

Department

ICTS (Institute of Clinical and Translational Sciences)

Additional Links

Supplemental material is available for this article at publisher site.