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This was done by conducting two different sensitivity analyses using plausible assumptions to impute missing participant event data for each trial.
To assess biological relevance of inferred regulatory network, we examined whether the identified TF-regulated transcriptional modules accumulate in certain Gene Ontology (GO) categories by conducting two different analyses: over-representation analysis and gene set enrichment analysis.
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We further demonstrate the biocompatibility and versatility of PFPE Tris by conducting three different biological reactions, namely, DNA polymeric nanoparticle production, enzyme detection with clinical samples, and cell cultures, in the PFPE Tris-based w/o microemulsions.
We conducted four different sets of experiments.
We conducted three different kinds of experiments.
Data loss was minimal, and reproducibility was met by conducting three separate experiments with three different healers under identical conditions, using two cell lines and three biological indicators of cell proliferation and viability.
Five studies were conducted by two different groups with common authors (three by Aurora [29 31], two by Bohoyin [32, 33]).
Experimental metastasis conducted by two different techniques, i.e., pretreatment and post-treatment models, showed the effectiveness of micellar formulations over plain drug to prevent the colonization of B16F10 cells in the lung.
Content analysis was conducted by two different researchers.
Enrichment analyses conducted by two different bioinformatics tools revealed a tissue specific profile of functional pathway perturbation.
For this study, although conducted by two different laboratories, the correlation between the two platform types (Affymetrix and Agilent) was only different for prostate stromal cells.
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