Quantitative comparison of the protein content of biological samples is a fundamental tool of research. The TMT and iTRAQ isobaric labeling technologies allow the comparison of 2, 4, 6, or 8 samples in one mass spectrometric analysis. Sound statistical models that scale with the most advanced mass spectrometry (MS) instruments are essential for their efficient use. Through the application of robust statistical methods, we developed models that capture variability from individual spectra to biological samples. Classical experimental designs with a distinct sample in each channel as well as the use of replicates in multiple channels are integrated into a single statistical framework. We have prepared complex test samples including controlled ...
The determination of protein changes related to stimuli such as pathological conditions is the core ...
Motivation: We introduce Census 2, an update of a mass spectrom-etry data analysis tool for peptide/...
Isobaric labeling is gaining popularity in proteomics due to its multiplexing capacity. However, cop...
Abstract Mass Spectrometry utilizing labeling allows multiple specimens to be subjected to mass spec...
The combination of stable isotope labeling (SIL) with mass spectrometry (MS) allows comparison of th...
The combination of stable isotope labeling (SIL) with mass spectrometry (MS) allows comparison of th...
Isobaric tagging techniques such as iTRAQ and TMT are widely used in quantitative proteomics and esp...
This study aimed to compare the depth and reproducibility of total proteome and differentially expre...
Abstract Background Liquid chromatography coupled with tandem mass spectrometry (LC-MS/MS) is widely...
Introduction: Quantitative proteomics using mass spectrometry is performed via label-free or label-b...
"Gel-free," or mass spectrometry (MS)-based, proteomics techniques are emerging as the methods of ch...
This dataset/code forms part of Andrew Landels' thesis: "Improving proteomic methods and investigati...
The combination of stable isotope labeling (SIL) with mass spectrometry (MS) allows comparison of th...
The multiplexing capabilities of isobaric mass tag based protein quantification, such as Tandem Mass...
Isobaric tags for relative and absolute quantitation (iTRAQ) is a prominent mass spectrometry techno...
The determination of protein changes related to stimuli such as pathological conditions is the core ...
Motivation: We introduce Census 2, an update of a mass spectrom-etry data analysis tool for peptide/...
Isobaric labeling is gaining popularity in proteomics due to its multiplexing capacity. However, cop...
Abstract Mass Spectrometry utilizing labeling allows multiple specimens to be subjected to mass spec...
The combination of stable isotope labeling (SIL) with mass spectrometry (MS) allows comparison of th...
The combination of stable isotope labeling (SIL) with mass spectrometry (MS) allows comparison of th...
Isobaric tagging techniques such as iTRAQ and TMT are widely used in quantitative proteomics and esp...
This study aimed to compare the depth and reproducibility of total proteome and differentially expre...
Abstract Background Liquid chromatography coupled with tandem mass spectrometry (LC-MS/MS) is widely...
Introduction: Quantitative proteomics using mass spectrometry is performed via label-free or label-b...
"Gel-free," or mass spectrometry (MS)-based, proteomics techniques are emerging as the methods of ch...
This dataset/code forms part of Andrew Landels' thesis: "Improving proteomic methods and investigati...
The combination of stable isotope labeling (SIL) with mass spectrometry (MS) allows comparison of th...
The multiplexing capabilities of isobaric mass tag based protein quantification, such as Tandem Mass...
Isobaric tags for relative and absolute quantitation (iTRAQ) is a prominent mass spectrometry techno...
The determination of protein changes related to stimuli such as pathological conditions is the core ...
Motivation: We introduce Census 2, an update of a mass spectrom-etry data analysis tool for peptide/...
Isobaric labeling is gaining popularity in proteomics due to its multiplexing capacity. However, cop...