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Optimal Range/Noise Level for Magnetic Sensor （AC Fluxgate）
For a project I have been tasked with developing a Magnetic Sensor that has a threshold of 0.1 ng. I’ve been reading through the datasheet for the Fluxgate sensor, and can’t seem to find any information about “optimal range” or “noise level”.
Is there any agreed upon way of determining what the optimal range and noise level for my device would be?
I’ve also looked at the ATOM-0 datasheet which makes a similar comment regarding the sensor. They go on to say that it is recommended to operate the sensor in the minimum/maximum output range when considering a noise reduction approach.
One approach is to use a tuned filter. You can tune this to give you a best SNR （signal to noise ratio） for a specific range of movement. This is ideal for a control loop. It relies on the fact that the range of movement you want to detect is well within the range of your filter. It means you don’t have to worry about harmonics or other spikes or resonances etc.
If you want to use this for a “raw” output （e.g. a fixed position threshold） then you have to invert it and try to find the point where your threshold makes the maximum or minimum signal. This is again an optimisation problem which is often approximated using the LMS （least mean squares） algorithm in an A/D converter.
In the end it comes down to the quality of your
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The Toll-like receptors （TLRs） are pattern recognition receptors mediating signalling upon the detection of microbial and viral products. The effects of these signalling molecules on immune cells are dependent on the context of disease and have been studied mainly in macrophages. Here, we investigate whether TLRs are also expressed in dendritic cells （DC）, which orchestrate immune responses during the initiation of immunity and are essential for the elimination of intracellular pathogens. We found that DC express high levels of both TLR7 and TLR8 transcripts, at least in vitro. The TLR7 agonist imiquimod induces DC activation and maturation. The TLR8-specific agonist CL075 enhances the maturation of DC in vitro. The level of TLR8 mRNA expression was significantly higher than that of TLR7, suggesting that the TLR
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