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Get LFQ Values for fractionated data at protein level #140
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Hi Annkatrin, The normalization coefficients are calculated internally when the "Normalize Intensities" option is selected. The reported protein intensities are derived from the normalized peptide intensities. There is no post-processing normalization required |
Here are my settings: Hey, here are my settings. So to get the intensity for a sample with fractions I simply sum all intensity values? |
Could you share your experimentalDesign.tsv file? |
FileName Condition Biorep Fraction Techrep |
Thanks for providing that. What make you say that the values appear to be wrong? Would it be useful if we provided the normalization coefficients as an output? |
If the intensities are already weighted I don't need the coefficients, but I think it would be still nice to report them somewhere. However, sometimes the summed LFQ values don't match the log2FC provided. Maybe it is worth checking. |
Hi,
I want to extract the protein LFQ intensities for fractionated data. I tried the sum but it appears to be wrong.
This paper (https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7563855/) states "FlashLFQ can normalize fractionated datasets by using a bounded Nelder–Mead optimizer [33] to find a normalization coefficient for each fraction, similar to MaxLFQ."
So I need to apply the normalization coefficient first to each fraction, but where are they listed?
I'm using the standard GALAXY output.
Best regards,
Annkatrin
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