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"Day_1_am_09_00_Vitek_Intro_Design.pdf" attached to page "Design and Analysis of Quantitative Proteomics Experiments"

MSSTATS Meena Choi, Olga Vitek College of Science College of Computer and Information Science OUTLINE • Methods: background • Linear mixed effects models • Evaluation • Spike-in and experimental datasets 2 MSSTATS • Statistical relative quantification of proteins and peptides • Which protein changes in abundance? • Complex experimental designs • Multiple conditions, factorial experiments,...

Generation of spectral library using Prosit

Hello Skyline Team, I am trying to use Prosit to generate spectral libraries and I realized that Prosit does not recognize "propionamide" as a fixed modification on the cysteine residues even when I set this modification on Skyline. Is there a way to modify the modifications into Prosit? Thanks for your help, Best, Benoit Do you have a hack that works for you with the Prosit website? If you...

Event Information

Dear Skyline Users: The Skyline Team is pleased to announce the Third Annual Skyline User Group Meeting, which will be held in Baltimore, MD on Sunday afternoon before ASMS.  We would like to thank the event sponsors (see below) for their generosity and interest in collaborating with the Skyline project on exciting new targeted and quantitative proteomics techniques.  Thanks to them, the meeting...

Skyline: great software tool

Skyline provides a great interface for the development and analysis of your MRM assays. Best way to find out is to try it yourself! Just a few statements about it: it's really user-friendly; you get started easily; the tutorials clearly explain the various possibilities; MRM assays can be prepared for different mass spectrometers; the various (graphical) representations to visually inspect your...

532 : X!Tandem in Skyline

open
Brendan MacLean
2017-07-15
Have you planned to install any search engine such as X!Tandem in Skyline? I miss to be able to carry out the entire pipeline in a friendly (as Skyline offers) way... Another thing, is skyline able to process pepXML files, with peptideProphet and iProphet analysis, from TPP?

Thank you
Nothing definite yet, but we will keep this on the TODO list, and it may happen in the future. Thanks for your interest.

525 : Results Grid or calibration curve

closed
2017-06-15
2018-10-15
Could it be possible to add in the results grid exclude standards and if possible zooming on the calibration curve to see the low end of the curve cause right now its not so friendly.
The "Exclude From Calibration" column got added to the Peptide Results in the Document Grid last year.

Great software.

Skyline is a very user-friendly, intuitive software tool that significantly speeds up my MRM-MS analysis. I particularly appreciate its compatibility with various MS platforms from different vendors and ease-of-use which make performing MRM assays using Skyline a smooth experience. Video tutorials and exceptional tech support are yet another great thing about this software. The usefulness of Skyline...

Webinar 20 (Marsh).pdf

Skyline Batch Instructions - Bruderer Skyline Batch Instructions.pdf - Google Drive Skyline Batch Ali Marsh Skyline Batch developer A user-friendly tool to run a simple Skyline workflow on many files at a time. Great for: • Overnight processing • Easily reprocessing data • Sharing workflows across computers • Quickly getting from a Skyline template to a report file https://drive.google.com...

Skyline is the ideal all-in-one solution for our targeted analysis of cell surface proteins

In our laboratory we increasingly move towards the targeted analysis of cell surface proteins. With the integration of Skyline into our SRM workflows, I think we found an ideal all-in-one solution that combines a user friendly interface with the necessary flexibility that is needed in our research environment. One of my preferred features is the easy generation and handling of large N glycopeptide...

Webinar 20 (Marsh).pptx

Skyline Batch Instructions - Bruderer Skyline Batch Instructions.pdf - Google Drive Skyline Batch Ali Marsh Skyline Batch developer A user-friendly tool to run a simple Skyline workflow on many files at a time. Great for: Overnight processing Easily reprocessing data Sharing workflows across computers Quickly getting from a Skyline template to a report file Download Files Skyline Batch Workflow...

581 : Usability idea: empty document should have getting-started hint text in the Targets window

open
Brian Pratt
2018-06-08
A common complaint I heard at ASMS this year is that Skyline is hard to get started with because "it just sits there with its blank screen and stares at you". We see this on the support board too ("I wanted to load my raw data but it said I didn't have any transitions, what now?").

Several users agreed that if the Targets window had some kind of help text in it when a document is empty, that would be a big help. No need to go full Clippy, but something friendly that suggests a few different ways to get targets loaded would be an inexpensive but large usability boost.
Not sure what this would look like, but Alex won't be the one to do it. Maybe just a clickable region that brings up the Start Page?

Opportunistic feature that will require the right inspiration to get done. No deadline.

129 : Clipboard failure in DataGridView

closed
2011-12-14
2014-04-10
Hi Nick,
We have started seeing a new unhandled exception in the DataGridView (details below). Can you look into how we can catch this exception, and show a more friendly error message?

Hopefully, we can catch it somewhere below the global handler, although I don't see any Skyline code on the current stack trace.

--Brendan


User comments:
I will save the file.

I tried to export a transitionlist with 90.000 transitions.

Jeppe

Skyline version: 1.1.1.3167
Installation ID: 588cf6a0-00ee-4e35-815e-cf8fa196f2f9
Exception type: System.Runtime.InteropServices.ExternalException
Error message: Requested Clipboard operation did not succeed.

Stack trace:
   at System.Windows.Forms.Clipboard.ThrowIfFailed(Int32 hr)
   at System.Windows.Forms.Clipboard.SetDataObject(Object data, Boolean copy, Int32 retryTimes, Int32 retryDelay)
   at System.Windows.Forms.DataGridView.ProcessInsertKey(Keys keyData)
   at System.Windows.Forms.DataGridView.ProcessDataGridViewKey(KeyEventArgs e)
   at System.Windows.Forms.DataGridView.OnKeyDown(KeyEventArgs e)
   at System.Windows.Forms.Control.ProcessKeyEventArgs(Message& m)
   at System.Windows.Forms.DataGridView.ProcessKeyEventArgs(Message& m)
   at System.Windows.Forms.Control.ProcessKeyMessage(Message& m)
   at System.Windows.Forms.Control.WmKeyChar(Message& m)
   at System.Windows.Forms.Control.WndProc(Message& m)
   at System.Windows.Forms.DataGridView.WndProc(Message& m)
   at System.Windows.Forms.Control.ControlNativeWindow.OnMessage(Message& m)
   at System.Windows.Forms.Control.ControlNativeWindow.WndProc(Message& m)
   at System.Windows.Forms.NativeWindow.Callback(IntPtr hWnd, Int32 msg, IntPtr wparam, IntPtr lparam)
What is the status on this?

Kristin Geddes

  Kristin Geddes received her B.S. in Clinical Laboratory Sciences from the University of Delaware. She began her career as Medical Technologist focused on Virology at the Children’s Hospital of Philadelphia. Kristin joined Merck Research Labs in 2006 and has developed analytical experience across a host of analytical platforms and a wide range of modalities, including small molecules, siRNA...

Robert Ahrends

  Robert Ahrends, Ph.D., is heading the lipidomics group at ISAS (ISAS, Dortmund, Germany). He received his Ph.D. in analytical chemistry, Humboldt University of Berlin. After his postdoc at Stanford Medical School, he started his own lab. Here his team focusses on global and signaling lipidomics in cardiovascular research such as the heart, platelets or fat cells. Their main interest is...

Is there any availiable tool for export skyline results and deal with the results?

I find the exported results format is just liake this: Protein Name Protein Accession Peptide Modified Sequence Point Count Protein Gene Replicate Name sp|A0AVT1|UBA6_HUMAN A0AVT1 M[+42]EGSEPVAAHQGEEASC[+57]SSWGTGSTNK 0 UBA6 500ng_1 sp|A0AVT1|UBA6_HUMAN A0AVT1 M[+42]EGSEPVAAHQGEEASC[+57]SSWGTGSTNK 0 UBA6 500ng_2 sp|A0AVT1|UBA6_HUMAN A0AVT1 M[+42]EGSEPVAAHQGEEASC[+57]SSWGTGSTNK...

633 : Usability idea: when we fail to open a Skyline document, check to see if it actually IS a Skyline document

closed
2019-02-28
2019-06-10
Lately we seem to get a lot of support requests where users are trying to just fire up Skyline then open a mass spec raw file. We issue an error like "the file contains an error at line 1 column 1", which only makes sense if the file is actually XML data.

Instead, we should:
 scan the first few hundred bytes to see if it contains "srm_settings" and "Skyline"
    if so, then throw that line/column error, fine.
 if not, see if we can identify it as mass spec data.
   if it is mass spec data, suggest they use File > Import Results, or if they don't have any targets, suggest they look into SeeMS.
Failing all that, issue an error like "this file does not appear to be a Skyline document."
Part of this is now implemented - we no longer just show the bare xml parser error. The bit about trying to identify raw data isn't there, but we do now offer a more friendly message about the file not being a skyline doc. Additionally if it's a .skyd file we'll find the .sky file next to it and load that without complaint.
Closing this - the important part is done, I doubt we'd ever get to the second half of this idea (about people trying to directly open raw data files instead of .sky files).
Just randomly looking at issues. The second part would be pretty easy for pwiz-recognized files. Just call ReaderList::identify on it and see if it returns non-empty. But that would add a ProteowizardWrapper dependency, where maybe you don't have one right now.

1056 : "Copy Data" for IMS heatmap display in Full Scan view is broken

open
Brian Pratt
2025-10-29
per https://skyline.ms/announcements/home/support/thread.view?rowId=72995

mauraisa (Members) created a new request    2025-10-28 13:38

I am trying use the "Copy Data" feature to copy the data from the "Full Scan" viewer that appears when you click on a chromotagram.

In general I think it is really useful to extract the underlying data from the visualizations in Skyline, however I am finding the way the output is formatted difficult to understand. What I would like to do is plot the data from the scan in R, but the format makes that difficult without moving a lot of things manually. At this point I am questioning whether the formatting is a feature or a bug.

I'm pretty sure the "Copy Data" feature is simply broken for scans with ion mobility data. I've attached a csv with the output that I am seeing when copying the data from a scan from a timsTOF. Columns for m/z and 1/K0 (Vs/cm^2) are repeated multiple times. It looks like the values for intensity are there but it not clear which rows they apply to. In row 3, 1/K0 (Vs/cm^2) is repeated in 57 columns.

I would think the best way to format the output would be a simple table with a single header and 3 columns: m/z, 1/K0 (Vs/cm^2), and intensity.

The first thing I tried to do was to look at what the output for a 2D scan without ion mobility data looks like. I think it a bit more comprehensible but still not very R/python friendly. There are 3 separate set of headers for each ion annotation.

Again I would think the best format would be a simple table with 3 columns: m/z, intensity, annotation.

Nathan Basisty

  Nathan Basisty Ph.D., is currently a tenure track Investigator at the NIA (NIH) and head of the Translational Geroproteomics Unit (TGU). He received his Ph.D., in Pathology and B.S. in Biochemistry from the University of Washington, where he investigated the role of protein turnover in mammalian aging and longevity using novel combinations of metabolic labeling, LC-MS/MS, and software tools....

Britt Lee

  Britt Lee My experiences from my graduate work, postdoc and industry are all focused in the small molecule and multiomics space, specializing in metabolomics, lipidomics, and proteomics. Now at Thermo Fisher Scientific, I focus on developing applications that advance omics research using cutting-edge mass spectrometry technologies. My work aims to bridge the gap between emerging analytical...

False identified transitions and product ions list

Hi Brenda, I imported data file of CE optimization (Agilent)and result as shown in the attachment. There are two questions: 1. As a practice, I added 4 synthetic peptides only but turned out identifying almost all 14 peptides list (green dot). But when I expanded those false identified transitions, it is actually noise level. So how can I set up a thershold noise level to avoid so many false idetifications?...