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. 2023 Mar 30;617(7961):564–573. doi: 10.1038/s41586-023-06003-w

Table 2.

PCR, metagenomics and viral WGS results from cases in which metagenomic sequencing was performed

Case ID Sample ID PCR Ct values Metagenomics reads Viral WGS coverage (10×)
DNA RNA
AAV2 HAdV HHV-6B AAV2 HAdV HHV-6B AAV2 HAdV HHV-6B AAV2 HAdV HHV-6B
Liver
1 JBL1 17 37 29 1,343 0 8 574 0 0 97 3
2 JBL4 21 42 32 360 0 8 49 0 0 93 2
3 JBL3 20 37 30 1,189 0 4 95 0 0 98 2
4 JBL2 20 37 27 1,564 0 203 42 0 0 98 94
5 JBL5 21 37 28 266 0 12 F F F
Blood
6a JBB14, JBB16, JBB9 24 36 37 151 0 0 77 0 0 95 35.5
7 JBB10, JBB11 21 36 37 103 0 0 F F F 49 F
8 JBPL1, JBB13 25 P/N −/N 277 0 0 165 0 0 94 F
9 JBB1 19 P/− P/− 1,936 5 0 0 0 0 94 F
10 JBB15 −/N N/N 37 0 0 0 F F F F

Where two results are shown, the first refers to the referring laboratory and the second to GOSH. Where there was a discrepancy, the positive result is shown. Where there is more than one sample for a single patient, Ct values represent the mean across the samples that were tested. De novo assembly of unclassified metagenomics reads was unremarkable. −, not tested (at GOSH due to insufficient residual material); F, failed; N, negative PCR result; P, positive PCR result in referring laboratory.

aFor metagenomics reads, the result of combining the datasets from two blood samples from the same case.