Comparative LC-MS is a powerful method for detailed quantitative comparison of complex protein mixtures. Dedicated software is required for detection, matching, and alignment of peaks in multiple LC-MS datasets. However, retention time shifts, saturation effects, limitations of experimental accuracy, and possible occurrence of split peaks make it difficult for software to perfectly match all chromatograms. We describe a procedure to assess the above problems and show that dataset quality can be enhanced with the aid of cluster analysis
Motivation: In a liquid chromatography–mass spectrometry (LC–MS)-based expressional proteomics, mult...
Motivation: Liquid chromatography coupled to mass spectrometry (LC-MS) and combined with tandem mass...
In recent years, mass spectrometry data analysis has become an important protein identification tech...
Comparative LC-MS is a powerful method for detailed quantitative comparison of complex protein mixtu...
Recently, liquid chromatography coupled to mass spectrometry (LC-MS) has become a standard technique...
Liquid chromatography coupled to mass spectrometry (LC-MS) is the dominant technological platform fo...
Motivation: The combination of liquid chromatography and mass spectrometry (LC/MS) has been widely u...
Retention time alignment is one of the most challenging steps in processing LC-MS datasets of comple...
Liquid chromatography coupled to mass spectrometry (LC-MS) is the dominant technological platform fo...
Liquid Chromatography Mass Spectrometry (LC-MS) based proteomics is an important tool in detecting c...
LC-MS/MS is an analytical technique used for protein identification and biomarker discovery. Typical...
In proteomic studies, liquid chromatography coupled with mass spectrometry (LC-MS) is a common platf...
This thesis reports techniques and optimization of algorithms to analyse label-free LC-MS data sets ...
Liquid chromatography-mass spectrometry (LC-MS) datasets can be compared or combined following chrom...
Liquid chromatography-mass spectrometry (LC-MS) datasets can be compared or combined following chrom...
Motivation: In a liquid chromatography–mass spectrometry (LC–MS)-based expressional proteomics, mult...
Motivation: Liquid chromatography coupled to mass spectrometry (LC-MS) and combined with tandem mass...
In recent years, mass spectrometry data analysis has become an important protein identification tech...
Comparative LC-MS is a powerful method for detailed quantitative comparison of complex protein mixtu...
Recently, liquid chromatography coupled to mass spectrometry (LC-MS) has become a standard technique...
Liquid chromatography coupled to mass spectrometry (LC-MS) is the dominant technological platform fo...
Motivation: The combination of liquid chromatography and mass spectrometry (LC/MS) has been widely u...
Retention time alignment is one of the most challenging steps in processing LC-MS datasets of comple...
Liquid chromatography coupled to mass spectrometry (LC-MS) is the dominant technological platform fo...
Liquid Chromatography Mass Spectrometry (LC-MS) based proteomics is an important tool in detecting c...
LC-MS/MS is an analytical technique used for protein identification and biomarker discovery. Typical...
In proteomic studies, liquid chromatography coupled with mass spectrometry (LC-MS) is a common platf...
This thesis reports techniques and optimization of algorithms to analyse label-free LC-MS data sets ...
Liquid chromatography-mass spectrometry (LC-MS) datasets can be compared or combined following chrom...
Liquid chromatography-mass spectrometry (LC-MS) datasets can be compared or combined following chrom...
Motivation: In a liquid chromatography–mass spectrometry (LC–MS)-based expressional proteomics, mult...
Motivation: Liquid chromatography coupled to mass spectrometry (LC-MS) and combined with tandem mass...
In recent years, mass spectrometry data analysis has become an important protein identification tech...