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. 2017 May 17;83(11):e00696-17. doi: 10.1128/AEM.00696-17

TABLE 2.

Effect of sample size on misclassifications

Sample size Ribosomal amplification Avg % FP ± SDa Avg % FN ± SDa
5,000 (1×)b Low 18.4 ± 0.6 20.2 ± 0.7
5,000 (1×) Medium 17.3 ± 0.7 19.4 ± 0.7
5,000 (1×) High 17.8 ± 0.7 20.4 ± 0.7
50,000 (10×) Low 14.7 ± 0.6 16.2 ± 0.6
50,000 (10×) Medium 13.2 ± 0.6 14.5 ± 0.6
50,000 (10×) High 15.3 ± 0.6 16.9 ± 0.6
500,000 (100×) Low 14.1 ± 0.6 14.5 ± 0.7
500,000 (100×) Medium 9.2 ± 0.6) 9.8 ± 0.5
500,000 (100×) High 14.0 ± 0.6 14.7 ± 0.6
5,000,000 (1,000×) Low 10.8 ± 0.7 10.8 ± 0.6
5,000,000 (1,000×) Medium 8.3 ± 0.6 8.4 ± 0.6
5,000,000 (1,000×) High 14.1 ± 0.7 14.1 ± 0.7
50,000,000 (10,000×) Low 10.7 ± 0.6 10.5 ± 0.7
50,000,000 (10,000×) Medium 8.1 ± 0.6 8.1 ± 0.6
50,000,000 (10,000×) High 14.0 ± 0.6 14.0 ± 0.7
a

The error rates are expressed as percentages of the populations that were detected in both DNA and RNA sampling profiles, and each value is the average of 100 independent iterations ± the standard deviation). With low sampling depths, the number of detected populations was less than the 5,000 input populations.

b

The parenthetical factors indicate the sampling depth as a multiple of the number of input populations (5,000) in the simulated community.