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. 2021 Oct 25;118(44):e2113065118. doi: 10.1073/pnas.2113065118

Table 2.

Confirmatory RT-qPCR analysis of SARS-CoV-2 DNA in COVID-19−positive samples

Sample number N1 N2 N4 ORF1ab −RevT/qPCR repeat −RevT/qPCR repeat +DNase
1 X X n/a n/a
2 X n/a n/a
3 X X n/a n/a
4 X n/a n/a
5 X
6 X
7 X (1/2)
8 X (1/2)
9 X (1/2)
10 X (2/2)
11 X X (2/2) X X (2/2)
12 X
13 X X (1/2)
14 X (1/2) X X (2/2) N2, N4
15 X N4
16 X (1/2) X (1/2)
17 X (1/2)
18 X (1/2)
19 X
20 X X (2/2) X X (2/2)
21 X X (2/2) X X (2/2)
22 X (1/2)

The qPCR for N1, N2, N4, and ORF1ab was repeated for all the samples with amplifications in the −RevT condition. Parentheses are for N2 and ORF1ab display repetition in technical qPCR replicates. An aliquot of −RevT samples was also used for DNase treatment prior to qPCR (last column) to show the DNA nature of possible −RevT signals (X indicates a detected amplification; — indicates no amplification detected; bolded results indicate possible virus genomic insertions; n/a indicates analysis was not performed).