Methods for the nalysis of data from clinical proteomic profiling studies. The focus is on the studies of human subjects, which are often observational case-control by design and have technical replicates. A method for sample size determination for planning these studies is proposed. It incorporates routines for adjusting for the expected heterogeneities and imbalances in the data and the within-sample replicate correlations.
|Bioconductor views||DifferentialExpression MultipleComparison OneChannel Preprocessing Proteomics|
|Maintainer||Stephen Nyangoma <[email protected]>|
|Package repository||View on GitHub|
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