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ENH reference the crappy QC data we made

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Nathan Dwarshuis 2021-09-07 00:12:35 -04:00
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@ -4699,12 +4699,11 @@ Using varying surface densities that are matched per-area between the beads and
\glspl{dms} we can then activate T cells and assess their growth/phenotype as a \glspl{dms} we can then activate T cells and assess their growth/phenotype as a
function of surface density and the presentation method. function of surface density and the presentation method.
% FIGURE this might warrant a better figure
\subsection{Reducing Ligand Variance} \subsection{Reducing Ligand Variance}
While we have robust quality control steps to quantify each step of the While we have robust quality control steps to quantify each step of the
\gls{dms} coating process, we still see high variance across time and personnel. \gls{dms} coating process, we still see high variance across time and personnel
This is less than ideal for translation. (\cref{fig:dms_coating}). This is less than ideal for translation.
When investigating the \gls{mab} and \gls{stp} binding, it appears that there is When investigating the \gls{mab} and \gls{stp} binding, it appears that there is
a significant variance both between and within different experiments (even a significant variance both between and within different experiments (even