PROSE: phenotype-specific network signatures from individual proteomic samples.
Bertrand Jern Han WongWeijia KongHui PengWilson Wen Bin GohPublished in: Briefings in bioinformatics (2023)
Proteomic studies characterize the protein composition of complex biological samples. Despite recent advancements in mass spectrometry instrumentation and computational tools, low proteome coverage and interpretability remains a challenge. To address this, we developed Proteome Support Vector Enrichment (PROSE), a fast, scalable and lightweight pipeline for scoring proteins based on orthogonal gene co-expression network matrices. PROSE utilizes simple protein lists as input, generating a standard enrichment score for all proteins, including undetected ones. In our benchmark with 7 other candidate prioritization techniques, PROSE shows high accuracy in missing protein prediction, with scores correlating strongly to corresponding gene expression data. As a further proof-of-concept, we applied PROSE to a reanalysis of the Cancer Cell Line Encyclopedia proteomics dataset, where it captures key phenotypic features, including gene dependency. We lastly demonstrated its applicability on a breast cancer clinical dataset, showing clustering by annotated molecular subtype and identification of putative drivers of triple-negative breast cancer. PROSE is available as a user-friendly Python module from https://github.com/bwbio/PROSE.
Keyphrases
- childhood cancer
- mass spectrometry
- gene expression
- binding protein
- genome wide
- protein protein
- copy number
- label free
- amino acid
- poor prognosis
- dna methylation
- liquid chromatography
- healthcare
- electronic health record
- squamous cell carcinoma
- big data
- rna seq
- deep learning
- artificial intelligence
- high performance liquid chromatography
- tandem mass spectrometry
- affordable care act
- papillary thyroid
- simultaneous determination