It looks like DESeq2 has been used efficaciously for MS data in published papers (https://www.ncbi.nlm.nih.gov/pubmed/?term=26193490). However, that is for unlabeled MS data, in which the only information is the spectral count. For labeled MS data, it does not appear DESeq2 is being used.
Thus we want to double check with you that Deseq2 is appropriate for labeled mass spectrometry counts. We will also greatly appreciated it if you could send us some publications in this area.
Thank you so much!
What's your take on normalization/computing offsets? I usually take the super naive approach of assuming that the assumptions underlying the methods used in DESeq2 or edgeR are +/- applicable to spectral count data, but given the unfortunate level of missingness (here I am talking about data that appear to be missing at random), I have never quite convinced myself that this is really a smart thing to do.