PRICE
PRICE identifies short open reading frames (sORFs) in eukaryotic cells by analyzing ribosome profiling (Ribo-seq) data to detect active translation.
Key Features:
- Noise Modeling: Implements noise modeling algorithms to account for and mitigate experimental noise in Ribo-seq data, improving sORF detection reliability.
- Resolution of Overlapping sORFs: Distinguishes overlapping sORFs to provide precise annotations of potential translation initiation sites and functional ORFs.
- Noncanonical Translation Initiation Detection: Identifies noncanonical translation initiation events beyond canonical start codons.
Scientific Applications:
- Antigen Repertoire Analysis: Through experimental validation using major histocompatibility complex class I (MHC I) peptidomics, identifies sORF-derived peptides that enter the MHC I presentation pathway.
- Functional Genomics: Maps sORFs to reveal previously unrecognized functional elements, informing studies of gene regulation and protein diversity.
- Translational Research: Supports investigation of noncanonical translation processes relevant to development, disease progression, and therapeutic interventions.
Methodology:
Integrates into the GEDI software platform; utilizes ribosome profiling (Ribo-seq) experiments to gather translational activity data; and applies noise modeling algorithms to refine data for sORF identification and characterization.
Topics
Details
- License:
- Apache-2.0
- Maturity:
- Mature
- Cost:
- Free of charge
- Tool Type:
- plugin
- Added:
- 5/29/2018
- Last Updated:
- 11/25/2024
Operations
Publications
Erhard F, Halenius A, Zimmermann C, L'Hernault A, Kowalewski DJ, Weekes MP, Stevanovic S, Zimmer R, Dölken L. Improved Ribo-seq enables identification of cryptic translation events. Nature Methods. 2018;15(5):363-366. doi:10.1038/nmeth.4631. PMID:29529017. PMCID:PMC6152898.
Documentation
Downloads
- Source codehttps://www.nature.com/articles/nmeth.4631#methods
- Source codehttps://github.com/erhard-lab/gedi