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Table 1 Quality metrics of pyrosequencing analysis

From: Structural variability and niche differentiation in the rhizosphere and endosphere bacterial microbiome of field-grown poplar trees

A. Total number of reads and read length before and after quality checking and trimming

Total # of raw reads before QC

341,915

Average read length before QC

405 ± 96

Total # of assigned reads after QC

204,723

Average read length after QC

207 ± 4

B. Assigned reads

Rhizosphere soil

Root

Stem

Leaf

Average # of reads

5058 ± 615

5311 ± 643

2761 ± 1174

3034 ± 960

Singletons (%)

26.09 ± 0.01a

5.01 ± 0.55b

2.60 ± 0.35b

2.21 ± 0.65b

Normalization to 2000 reads per sample

C. Non-target rRNA (%)

Rhizosphere soil

Root

Stem

Leaf

Chloroplast/plastid

0

0.01 ± 0.01

0.44 ± 0.17

0.03 ± 0.02

Mitochondria

0

0

0

0

Archaea

0.03 ± 0.01

0

0

0

D. Unclassified reads

Rhizosphere soil

Root

Stem

Leaf

Reads (%)

34.07 ± 1.10a

4.74 ± 0.32b

19.05 ± 4.32b

3.59 ± 1.03b

  1. A: Quality metrics before and after quality control (QC), the average read length was calculated based on 52 samples across all plant compartments. B: Average number of assigned reads (± standard deviation) per plant compartment and percentages of singleton reads (± standard deviation). Numbers of singletons were statistically compared using one-way ANOVA and Tukey’s Honest significant differences post hoc tests. Statistical differences at the 95% confidence interval are indicated with lowercase letters. C: Comparison of the number of non-target 16S rRNA sequences (%) co-amplified during PCR amplification. and D: Reads that could not be unambiguously classified at the phylum level (“unclassified”) (%). Each plant compartment is evaluated separately and data represent 15 biologically independent replicates (± standard deviation) for the rhizosphere soil and root endosphere samples and 11 biologically independent replicates (± standard deviation) for the stem and leaf endosphere samples