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Wrap the sample in the sample paper.
Overall microbiomes (rarefied to 24,509 reads for each sample) as well as the community of locally stable microbial associates (OTUs present in 100% of the samples at each sampling location; rarefied to 23,940 reads for each sample) and the core microbiome (OTUs present in all samples; rarefied to 23,890 reads for each sample) were determined.
For each sample, qPCRs were performed in technical triplicate.
Each target was ran in triplicate for each sample.
We performed RNA sequencing in duplicate for each sample.
Samples were analyzed in triplicate and mean ± SD for each sample is shown.
For the sample with fluence 5 × 1017/cm2, only 1% to 2% of Fe4N + Fe4−xNixN exists in the sample.
Samples were kept in the auto sampler set to 4 °C.
Cell samples are diverse in nature and a new ground truth may be needed for each new sample.
For the transcriptome analysis each sample was handled in triplicate.
A sample question in the survey.
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