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ABSTRACT: Background
High throughput proteomics has enabled hypothesis free biomarker discovery. However, differences in sample sizes, biological fluid, and quantification technologies have limited replication and validation of the results, and studies on the cross-platform variability are lacking. Here, we present the first orthogonal validation across three platforms in Parkinson's disease (PD) to understand the technical and biological challenges of proteomic studies.Methods
We have leveraged publicly available proteomic data from cerebrospinal fluid (CSF), plasma, and urine within the Parkinson's Progression Markers Initiative (PPMI) cohort, generated using SomaScan5K (CSF), mass spectrometry (MS; CSF, plasma, and urine), and Olink Explore (CSF and plasma). Across platforms, we c
SUBMITTER: Kumar R
PROVIDER: S-EPMC12485981 | biostudies-literature | 2025 Sep
REPOSITORIES: biostudies-literature