Mass spectral data collected in DDA mode, MS/MS scan as IT, fragmentation mode CID, use pfind to read RAW. format files, 12 samples were tried, and the number of matching peptides and proteins was always 0, in other software there are 300+ matching peptides, and I feel that there is a problem with the data reading. I would like to ask the teacher where the problem is and how to solve it.
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