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All tissues were sampled in duplicate.
Each chronic wound site was sampled in duplicate for parallel testing.
Cultures were sampled in duplicate for each time point, total RNA extracted, and each sample sequenced via an individual lane of Illumina sequence determination.
Each tumor was sampled in duplicate from representative areas using a 0.6-mm punch, yielding composite array blocks comprising a total of 584 tissue cores.
In this study, 125 tubewells 6−36 m deep were sampled in duplicate for 18 months to quantify the presence of the fecal indicator Escherichia coli.
Each tumour was sampled in duplicate from representative areas using a 0.6-mm punch, yielding composite array blocks comprising a total of 568 tissue cores.
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It is common practice to run samples in duplicate to ensure a good reproducibility.
Apparent amylose content was determined on the samples in duplicate by the simplified iodine assay method (Juliano 1971).
In the assay, standards of T4 were applied in triplicate, and samples in duplicate.
Samples in duplicate or triplicate and standards were incubated in the wells overnight at 4°C.
Q-PCR analysis was performed on immunoprecipitated and un-enriched input DNA samples in duplicate.
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