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. 2022 Jul 7;10(4):e01755-22. doi: 10.1128/spectrum.01755-22

TABLE 3.

Overview of important parameters for each sequencing run

Before removing nonbacterial reads
After removing nonbacterial reads
Run No. reads No. reads pPNAa No. reads mPNAb No. reads No. reads pPNAa No. reads mPNAb No. samples No. taxac Avg library size % nonbacterial Sample typesd PCR conditions
Run 1 5E+06 4E+06 5E+05 9E+04 0 0 85 1,289 1,033 96.6 P No clamps
Run 2 5E+05 6E+03 3E+05 6E+04 0 2 94 761 1,089 81.0 P pPNA clamps
Run 3 1E+05 1E+03 3E+02 1E+05 0 0 12 142 9,487 3.29 I No clamps
Run 4 8E+04 1E+03 2E+03 6E+04 0 0 58 761 1,114 39.6 P pPNA and mPNA clamps
Run 5 1E+05 0E+00 0E+00 1E+04 0 0 7 377 20,569 0.0 I No clamps
a

The number of reads compatible with plastid peptide nucleic acid (pPNA) clamps.

b

Mitochondrial peptide nucleic acid (mPNA) clamps.

c

Number of different amplicon sequence variants (ASVs)

d

Sample types included in the run (P = phyllosphere samples, I = invertebrate samples).