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All genes represented by the array showed a single peak on the melting curve characteristic of the specific products.
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Average DNA methylation and genotypes were determined using Epigenetic Sequencing MEthylation (ESME) analysis software [ 33]. β values determined by ESME and the HumanMethylation450 array showed a high, positive correlation (R = 0.8217).
As indicated in Figure 2A, the parental NCI-H929 did not express TNF- α, but an analysis by PCR array showed that NCI-H929 rather expressed IL-8, another proinflammatory cytokine.
Analysis by cytokine array showed a negligible signal for IL-10 and IL-9 in a pool of three splenic tumour tissue samples, which was equivalent to NSC splenic samples.
Finally, a genetic classification of lung ADC by CGH array showed that EGFR mutated tumors could be individualized as a specific cluster [ 27].
Assessment of gene copy number variations in these tumours by CGH array showed gene copy number variations that could potentially lead to PI3K/Akt/mTOR pathway activation.
Extracellular matrix expression as determined by ECM PCR array showed differences (Fig. 5c).
The unit population sampled by a four-tetrode array showed more homogeneous distribution than those sampled by an eight-microelectrode array.
Gene expression as determined by pluripotency-specific PCR array showed no differences between undifferentiated samples of hESC and phESC (Fig. 2a).
The clonal frequencies measured at day 3 were in agreement with the expansion measured by the T-array, showing that the T-array protocol quantitatively detects clonal expansion.
Alterations in pulmonary gene expression by a custom designed TaqMan array showed minimal differences between the fumes at 4 h.
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