MAPDIA
MAPDIA performs statistical analysis of differential protein expression using fragment-level intensities from Data Independent Acquisition (DIA) mass spectrometry.
Key Features:
- Intensity Normalization: Provides total intensity sum normalization and local intensity sum normalization in retention time space to adjust fragment-level intensities across samples.
- Peptide/Fragment Selection: Identifies and retains peptides and fragments that preserve major quantitative trends while removing outlier observations across samples.
- Statistical Analysis: Implements hierarchical model-based statistical significance analysis for protein-level differential expression, supporting multi-group comparisons and control of false discovery rates using selected peptides and fragments.
Scientific Applications:
- Simulation Validation: Validated on comprehensive simulation datasets to assess detection of differentially expressed proteins.
- 14-3-3β Dynamic Interaction Network: Applied to DIA datasets characterizing the 14-3-3β interaction network and its dynamics.
- Prostate Cancer Glycoproteome: Applied to DIA datasets to analyze proteomic alterations in the prostate cancer glycoproteome.
Methodology:
The workflow comprises normalization of fragment-level intensities (total and local intensity sum in retention time space), peptide/fragment selection with outlier removal and trend preservation, and hierarchical model-based statistical significance analysis for multi-group protein-level differential expression with false discovery rate control.
Topics
Collections
Details
- Tool Type:
- command-line tool
- Operating Systems:
- Linux, Windows, Mac
- Programming Languages:
- C++
- Added:
- 8/3/2017
- Last Updated:
- 11/25/2024
Operations
Data Inputs & Outputs
Spectral analysis
Outputs
Publications
Teo G, Kim S, Tsou C, Collins B, Gingras A, Nesvizhskii AI, Choi H. mapDIA: Preprocessing and statistical analysis of quantitative proteomics data from data independent acquisition mass spectrometry. Journal of Proteomics. 2015;129:108-120. doi:10.1016/j.jprot.2015.09.013. PMID:26381204. PMCID:PMC4630088.