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. 2022 Nov 21;227(7):888–900. doi: 10.1093/infdis/jiac450

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© The Author(s) 2022. Published by Oxford University Press on behalf of Infectious Diseases Society of America.

This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (https://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com

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Figure 4. — NGS coverage in urine and plasma samples. NGS was performed from longitudinal urine (n = 77) and plasma samples (n = 29) from the 20 hematopoietic cell transplantation patients using amplicons with different lengths (250 bp, 1000 bp, and 5000 bp). A, Targeted NGS from urine using different amplicon targets. B, Targeted NGS from plasma using different amplicon targets. C, NGS coverage of full BKPyV genome sequences from urine samples using 250-bp, 1000-bp, and 5000-bp targets (n = 63). Abbreviations: BKPyV, BK polyomavirus; NGS, next-generation sequencing; no, no target amplicon present; yes, target amplicon present.