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Factor in amplification efficiency #21
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So I tried a workaround myself, maybe you might have an Idea how to implement it better. I modified the "pcr_ddct" function to also take a dataframe of amplification efficiencies as Input (which I reformatted from the output of pcr_assess to only include the genes as columns with one row where the amplification efficiency is stored). I then added a variable "y" to the function that sets "res", which uses the variable "x" to get the column name of the column with the values in "x":
and called a modified version of the ".pcr_relative" function with the addition of the amplification_efficiency dataframe and the column name:
The modified function looks like this:
It uses the column name (gene name) stored in "y" to get the associated amplification efficiency of the gene from the dataframe and uses that as the base instead of the "2" in the original function. What are your thoughts on this approach? Best regards, Richard |
Thanks, @richardstoeckl for reaching out, and sorry for the late reply. |
Hi,
thank you for your very useful package!
In your publication you mention the ability to factor in less-than-perfect amplification efficiencies in a future version of this package.
Sadly, I was not able to find this option.
Is this feature still in development?
Greetings, Richard
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