Proteomics experiment on Listeria monocytogenes strains ScottA was performed in biological triplicates (control, high osmolarity, low pH, bile), except for EGD-e bile, where we could only quantify duplicates. All Listeria data sets data were analyzed using Spectronaut v12 (Biognosys) using standard settings (dynamic peak detection, automatic precision nonlinear iRT calibration, interference correction, and cross run normalization). Results were filtered for a qvalue of 0.01 on the peptide level. Peptides for protein group quantitation were selected using Qvalue (only individual values passing the qvalue threshold of 0.01 were considered, NAs in data matrix) without imputation. MSstats v3.12 was used for differential abundance analysis. R script is available in the ‘methods’ folder.
[doi:10.25345/C50X63]
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Keywords: MassIVE.quant reviewed - Platinum
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