Before I export my data from Skyline for data analysis, I have the following final things to do:

  • Adjust peak boundaries
  • Determine if any .raw files should be discarded, based on poor-quality data and those that I re-ran & re-made
  • Look @ all blank runs to see if there are any weird signals
  • Check out blank samples

Adjusting peak boundaries

Some helpful keyboard shortcuts:

  • Scroll between replicates: Ctrl+Up or Ctrl+Down
  • Auto-zoom to best peak: F11
  • Un-autozoom out from best beak: Shift+F11

Some transition peaks look poor, but they are present. Here is an example of replicate data for the Superoxide Dismutase protein, showing the overall view and the zoomed view:

This is in comparison to the following replicate, where there is no peak present betwen RT 14-15:

Not sure what to do in the situation where a peak is split into 2 peaks (as below); Skyline opted for the boundaries to encompass both peaks. I will do the same, as the total RT for both peaks appears to be similar to that of other reps:


  • Poor quality reps: 178, 254, 208, 212, 213, 297_170728020436,
  • A peptide with RT ~18 must be co-eluting, as it pops up in a few res/peptides. Perhaps it is the [PEPTIDE W/ 18], that gets stuck in the column and pops up. For example, the following is a zoomed-out view of Ras-related protein peptide, which should have it’s peak around 22.7. This is rep #254, but it pops up in lots of reps:
    A couple peptides elute @ ~18min, and could be the culprit: Sodium/potassium-transporting ATPase subunit alpha-4, MVTGDNVNTAR; Catalase, LYSYSDTHR;

Total actions performed on SRM data in Skyline:

  • Removed peaks from replicates where no peak was present @ designated retention time (as per DIA/SRM regression). Replications w/ no peaks for peptides will be represented as #N/A when data is exported.
  • ID’d peptides with very poor data across multiple replicates; I may not use these peptides in my analysis; TBD. See peptides in red
  • Adjusted retention time boundaries for all reps all peptides. I erred on NOT adjusting boundaries if they looked OK to maintain consistency.
  • ID’d and deleted 2 transitions that do not align with other transitions at designated RT. Transitions are:
    • Superoxide dismutase, TIVVHADVDDLGK, y4
    • Ras-related protein Rab-11B VVLVGDSGVGK, y4
  • Documented peptides and transitions w/ poor quality over several samples here

Exported data from Skyline:

Export -> Report, then I edited the Transition Results report with the following metrics: Protein Name, Transitions, Peptide Sequence, Fragment Ion, Peptide Retention Time, Area; I selected “Pivot Replicate Name”. Here’s a preview of the report:

I then exported the same report, NOT pivoted by replicate name.

Both files were uploaded to my Geoduck-DNR/Data repo:

SRM Transition Results, pivoted
SRM Transitoin Results, not pivoted

from LabNotebook

Cleaning up SRM data in Skyline, part II
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