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Tested the effect of setting F_PL using values taken from the mean after equilibration from a previous run of assaytools, and dF_PL=0.50, which was approximated from the standard deviation. Tested this for Src:Erlotinib and Src: Gefitinib.
Similar to issue #106 we see an expected removal of long tails and better reproducibility compared to without setting the F_PL. Note here, we are still looking at a dPstated = 0.35 * inputs['Pstated'].
Without setting F_PL:
Setting F_PL and dF_PL:
Without setting F_PL:
Setting F_PL and dF_PL:
Also we no longer see any sort of correlation between F_PL and DeltaG:
Without setting F_PL:
Setting F_PL and dF_PL:
While this is nice, I'm worried this is maybe too restrictive? Maybe we can just have a slightly more informed prior instead of this (link):
Can you show this to Nick? We might ask his thoughts on using an estimate of F_PL and its uncertainty from our spectra assay and/or a separate cuvette assay.
Tested the effect of setting
F_PL
using values taken from the mean after equilibration from a previous run of assaytools, anddF_PL=0.50
, which was approximated from the standard deviation. Tested this for Src:Erlotinib and Src: Gefitinib.Similar to issue #106 we see an expected removal of long tails and better reproducibility compared to without setting the
F_PL
. Note here, we are still looking at adPstated = 0.35 * inputs['Pstated']
.Without setting
F_PL
:Setting
F_PL
anddF_PL
:Without setting
F_PL
:Setting
F_PL
anddF_PL
:Also we no longer see any sort of correlation between F_PL and DeltaG:
Without setting
F_PL
:Setting
F_PL
anddF_PL
:While this is nice, I'm worried this is maybe too restrictive? Maybe we can just have a slightly more informed prior instead of this (link):
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