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. 2025 Dec 19;16:2952. doi: 10.1038/s41598-025-32771-8

Table 1.

Summary of sample sets used in this study. All AIV isolates have been ascribed AIV subtypes.

Sample set name Source Sample size Used for evaluating
Sample set 1 AIV isolates from NZWBAIS n = 12 Whole-genome amplification on Bento Lab Pro (Bento Bioworks Ltd), AIV amplicon profile on Invitrogen E-gel Power Snap Electrophoresis System (Thermo Fisher)
Sample set 2 AIV swabs from NZWBAIS n = 37 Influenza A RT-qPCR assay on MIC PCR system (Bio Molecular Systems)
Sample set 3 AIV swabs from Otago poultry farm infected with HPAI H7N6 n = 5 Influenza A RT-qPCR assay on MIC PCR system (Bio Molecular Systems), RNA extraction kits on the Bento Lab Pro (Bento Bioworks Ltd)
Sample set 4 AIV isolates from NZWBAIS n = 7 QIAamp Viral RNA Mini Kit (Qiagen) on the portable system
Sample set 5 AIV isolates from NZWBAIS n = 3 Zymo Quick-Viral RNA Kit (Zymo Research) on the portable system
Sample set 6 AIV swabs from NZWBAIS n = 45 Full portable system
Sample set 7 Antarctica n = 5 Full portable system in the field