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We performed a microarray experiment with a 2×2 factorial design to profile gene expression in human NK cells (Velasquez et al., 2016) [1].
To systematically investigate the body-fluid-specific expression of mRNAs and find novel mRNA markers for forensic body fluid identification, we performed DNA microarray experiment with 24 Korean body fluid samples.
We compared the genes differentially regulated in our microarray experiment with Rubin's list of genes essential for in vitro growth and for growth within macrophages.
For simplicity, we focus on two-gene interactions in a microarray experiment with expression profiles from samples in two classes, e.g. presence and absence of a disease.
We first identified a study, in which the gene expression profiles of 35 human tissue types were also established using a cDNA-based microarray experiment with a common reference design [7].
To gain an understanding of the roles played by IKAP in neuronal cell growth and differentiation, we carried out a DNA microarray experiment with RNA extracted from two cell lines of SHSY5Y cells: i) IKAP-DR, in which IKAP expression was Down Regulated by an shRNA against the IKBKAP gene and ii) control cells transfected with the empty vector.
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This finding is of major importance for the interpretation and design of future microarray experiments with adult Daphnia.
We illustrate the inference technique to obtain the value of the parameter p from microarray experiments with a specific example.
Microarray experiments with at least 2 replicates were taken.
We kept the genes which have microarray experiments with at least 3 replicates.
This method, however, does not discriminate between individual microarray experiments with or without associated biases.
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