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The reliability of chip assay was confirmed by signaling scatter graph and RT-PCR (Figures 5A and 5B).
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To verify the reliability of our ChIP-on-chip results, the method of ChIP-qPCR was used to detect the promoter sequences of randomly selected genes in samples of our output DNA.
In order to verify the reliability of the ChIP-on-chip results, qPCR was used to detect the promoter sequences of selected genes in ouput DNA fractions from CHB patients and healthy controls.
Six genes from the different categories of differentially expressed genes were chosen to further verify the reliability of the chip results by real time RT-PCR using the DNA-binding dye SYBR green I according to the manufacturer's instructions.
Further, we used qPCR to confirm the reliability of miRNA chip in knocking down the expression of PDCD4 in NPC cells.
Notably, most reported AICD-regulated genes were also found in our ChIP-seq data, representing robust controls for verifying the reliability of our ChIP-seq data (Supplementary Table S3).
Soft errors resulting from alpha-particle strikes are one of the major factors that reduces the reliability of memory chips.
Previous work based on the vulnerability factor (VF) analysis proposed analytical models to evaluate the reliability of on-chip data and instruction caches.
The experiments do coincide with the simulative prediction with good accuracy, allowing for the first time a distinct statement about the reliability of flip-chip packages with attached heat-spreaders.
It is demonstrated that employing an optimum-radiation phased array antenna and multihop communications will increase the reliability of on-chip wireless links by several orders of magnitude using a limited power budget less than 0.1 pJ/bit.
The results of the influence of lead-free solder paste, design and process parameters on the attachment reliability of chip surface-mounted components (SMCs) on thick-film conductor pads are presented.
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