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Use of a High Affinity DNA Ligand in Flow Cytometry Ncbi Nlm Nih Form

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so let's move to the last unit i wanted to talk about here which is now that we've got a big pile of well-calibrated flow cytometry data what do we want to do to visualize and interpret it so let's start with a reminder that we're going to be thinking about things not in terms of ordinary means and standard deviations but in terms of geometric statistics which are essentially means and standard deviations on the log scale you may have noticed that almost every graph that i've shown so far is using log scale axes um and that's because um our cell expression tends to be uh bell curves on the log scale and there's a reason for this this comes down to essentially that anything to do with gene expression can be thought about as a complex reaction with a whole bunch of rates being multiplied for all the stuff that we usually don't model like the actual uh transcription and translation processes which when you multiply a bunch of

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Use of a High Affinity DNA Ligand in Flow Cytometry Ncbi Nlm Nih Form

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How to create an eSignature for the use of a high affinity dna ligand in flow cytometry ncbi nlm nih

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