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It said both methods had a role.
Both methods had a modest number of reads that failed taxonomic assignment because the read's sequence identity to the reference organism was below the stringent identity threshold (316 Enz+Sanger reads, between 791 and 2932 Enz+pyrosequencing reads).
Both methods had a success rate of 100%.
Both methods had a limit of detection of 0·03 g/100 g.
Both methods had a low true positive rate, false positive rate, and F-score.
Those patients who were HER2-negative by both methods had a pCR rate of only 20%.
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Both methods had an accuracy of over 90% before day 84, which was several weeks from the mean peak day; day 121 for moderate epidemics.
The panel said both methods have a role.
Both methods have a median of 8/10, but we find more instances of simulations for which only 2 5 dysregulated genes were identified with inference.
Both methods have a very low cost are easy to administer do not require a sleep centre (unlike, eg, polysomnography), and can be self-administered.
The films obtained by both methods have a better photocatalytic activity in the degradation of RB5 compared to MG due to the weaker NN bond in comparison with the CC bond between the central carbon atom and N,N-dimethylaminobenzyl in MG.
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