|Title||»||Heavy/Light Peptide Chromatogram Import Range Discrepancies|
|Assigned To||Guest||»||Brendan MacLean|
I have imported a Thermo RAW DDA file in order to setup a scheduled PRM run. I have the Full-Scan settings to import all matching scans and "Synchronize Zooming" is also selected. I find that there are many cases where different retention time ranges are imported for heavy and light peptides, in some cases resulting in the peak of interest being absent in one of the channels (see attached /Powerpoint slides).
Is there a setting or a conflict I may be overlooking? Thanks.