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Progenesis LC-MS

A unique approach for label-free LC-MS data analysis
Quantify and identify the significant proteins in your experiment…

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The Progenesis LC-MS package has enabled our service lab customers to be taught in a very short time how to extract reliable results with they are happy.

Peter James
Prof. of Protein Technology, Lund University, Sweden

How is normalisation performed in fractionated LC-MS experiments?

In any LC-MS experiment each run will be effected by systematic errors (e.g. sample loading differences) which will add bias to a quantitative analysis. The purpose of normalisation is to calculate a correction factor which will compensate for these systematic errors.

For fractionated experiments the correction happens in 2 parts. First, we calculate a within-fraction normalisation factor for each run and then a between-fraction normalisation factor for each fraction. Normalised feature abundances for each run are then given as the raw abundances multiplied by the appropriate 2 factors for that run.

The within-fraction normalisation factors are calculated in the first phase of the analysis in which each fraction is analysed separately.

The between-fraction normalisation factors are calculated in the recombine fraction part of the workflow so as to make the mean log normalised abundances equal for each fraction.