Background: Spectral counting methods provide an easy means of identifying proteins with differing abundances between complex mixtures using shotgun proteomics data. The crux spectral-counts command, implemented as part of the Crux software toolkit, implements four previously reported spectral counting methods, the spectral index (SIN), the exponentially modified protein abundance index (emPAI), the normalized spectral abundance factor (NSAF), and the distributed normalized spectral abundance factor (dNSAF). Results: We compared the reproducibility and the linearity relative to each protein’s abundance of the four spectral counting metrics. Our analysis suggests that NSAF yields the most reproducible counts across technical and biological r...
International audienceInferring protein abundances from peptide intensities is the key step in quant...
Identifying proteins in cell extracts by shotgun proteomics involves digesting the proteins, sequenc...
Differentiating and quantifying protein differences in complex samples produces significant challeng...
The measurement of change in biological systems through protein quantification is a central theme in...
A major goal in proteomics is the comprehensive and accurate description of a proteome. This task in...
Abstract Background Mass spectrometry (MS) based label-free protein quantitation has mainly focused ...
The measurement of change in biological systems through protein quantification is a central theme in...
How to process and analyze MS data to quantify and statistically compare protein abundances in botto...
Mass spectrometry (MS) based label-free protein quantitation has mainly focused on analysis of ion p...
There is a great interest in reliable ways to obtain absolute protein abundances at a proteome-wide ...
High-throughput techniques are currently some of the most promising methods to study molecular biolo...
Label-free shotgun mass spectrometry enables the detection of significant changes in protein abundan...
Spectral counting is a straightforward label-free quantitation strategy used in bottom-up proteomics...
Although protein expression is regulated both temporally and spatially, most proteins have an intrin...
During the recent years, Liquid chromatography-mass spectrometry (LC-MS) has gained enormous attenti...
International audienceInferring protein abundances from peptide intensities is the key step in quant...
Identifying proteins in cell extracts by shotgun proteomics involves digesting the proteins, sequenc...
Differentiating and quantifying protein differences in complex samples produces significant challeng...
The measurement of change in biological systems through protein quantification is a central theme in...
A major goal in proteomics is the comprehensive and accurate description of a proteome. This task in...
Abstract Background Mass spectrometry (MS) based label-free protein quantitation has mainly focused ...
The measurement of change in biological systems through protein quantification is a central theme in...
How to process and analyze MS data to quantify and statistically compare protein abundances in botto...
Mass spectrometry (MS) based label-free protein quantitation has mainly focused on analysis of ion p...
There is a great interest in reliable ways to obtain absolute protein abundances at a proteome-wide ...
High-throughput techniques are currently some of the most promising methods to study molecular biolo...
Label-free shotgun mass spectrometry enables the detection of significant changes in protein abundan...
Spectral counting is a straightforward label-free quantitation strategy used in bottom-up proteomics...
Although protein expression is regulated both temporally and spatially, most proteins have an intrin...
During the recent years, Liquid chromatography-mass spectrometry (LC-MS) has gained enormous attenti...
International audienceInferring protein abundances from peptide intensities is the key step in quant...
Identifying proteins in cell extracts by shotgun proteomics involves digesting the proteins, sequenc...
Differentiating and quantifying protein differences in complex samples produces significant challeng...