Two-dimensional gel electrophoresis is a major technique in global analysis at the proteinlevel. This paper presents an examination of spot volume data from three gel sets with radioactivelylabeled yeast Saccharomyces cerevisiae proteins. A strong variance versus meandependence in data was found to be stabilized by applying a shifted logarithmic transformation.However, transformed data showed a remaining substantial variance heterogeneity fordifferent proteins. Furthermore, examination of studentized residuals revealed that transformeddata were approximately normally distributed and that there were spatial correlationsamong the measurement errors in the gel
International audienceTwo-dimensional gel electrophoresis has been instrumental in the development o...
After separation through two-dimensional gel electrophoresis (2-DE), several hundreds of individual ...
Quantitative proteomic studies, based on two-dimensional gel electrophoresis, are commonly used to f...
An interlaboratory comparison was conducted on the positional and quantitative reproducibility of ye...
For the development of valid algorithms for matching protein spots between two-dimensional gels, it ...
Two-dimensional gel electrophoresis is a biochemical technique that combines isoelectric focusing an...
International audienceTwo-dimensional gel electrophoresis has been instrumental in the development o...
The relationship between spot volume and variation for all protein spots observed on large format 2D...
Two-dimensional gel electrophoresis (2-DE) is one of the most powerful methods for studying global p...
Two-dimensional Dierence Gel Electrophoresis (DIGE) circumvents many of the prob-lems associated wit...
Comparing different proteomes by classical two-dimensional electrophoresis is challenging and often ...
The strategies and methods used by the QUEST system for two-dimensional gel analysis are described, ...
In this study, we examined yeast proteins by two-dimensional (2D) gel electrophoresis and gathered q...
Two-dimensional (2-D) gel electrophoresis is often used in proteome projects to provide a global vie...
Two-dimensional SIDS-PAGE gel electrophoresis using post-run staining is widely used to measure the ...
International audienceTwo-dimensional gel electrophoresis has been instrumental in the development o...
After separation through two-dimensional gel electrophoresis (2-DE), several hundreds of individual ...
Quantitative proteomic studies, based on two-dimensional gel electrophoresis, are commonly used to f...
An interlaboratory comparison was conducted on the positional and quantitative reproducibility of ye...
For the development of valid algorithms for matching protein spots between two-dimensional gels, it ...
Two-dimensional gel electrophoresis is a biochemical technique that combines isoelectric focusing an...
International audienceTwo-dimensional gel electrophoresis has been instrumental in the development o...
The relationship between spot volume and variation for all protein spots observed on large format 2D...
Two-dimensional gel electrophoresis (2-DE) is one of the most powerful methods for studying global p...
Two-dimensional Dierence Gel Electrophoresis (DIGE) circumvents many of the prob-lems associated wit...
Comparing different proteomes by classical two-dimensional electrophoresis is challenging and often ...
The strategies and methods used by the QUEST system for two-dimensional gel analysis are described, ...
In this study, we examined yeast proteins by two-dimensional (2D) gel electrophoresis and gathered q...
Two-dimensional (2-D) gel electrophoresis is often used in proteome projects to provide a global vie...
Two-dimensional SIDS-PAGE gel electrophoresis using post-run staining is widely used to measure the ...
International audienceTwo-dimensional gel electrophoresis has been instrumental in the development o...
After separation through two-dimensional gel electrophoresis (2-DE), several hundreds of individual ...
Quantitative proteomic studies, based on two-dimensional gel electrophoresis, are commonly used to f...