DeepShape
DeepShape estimates isoform-level ribosome abundance and distribution from ribosome profiling (Ribo-seq) data using a deep learning model that operates without RNA-seq input.
Key Features:
- Isoform-Level Precision: Assigns multiple-mapped Ribo-seq reads to similar isoforms to enable isoform-specific ribosome abundance and profile estimation.
- Deep Learning Integration: Employs a deep learning model to simultaneously estimate ribosome abundance and compute ribosome profiles for each isoform.
- RNA-seq Independence: Estimates transcript-level ribosome metrics without requiring RNA-seq data for transcript abundance.
- Codon Residence Index (CRI): Introduces CRI as a metric that measures the relative speed at which ribosomes traverse a codon compared to its synonymous counterparts.
Scientific Applications:
- PC3 cell PP242 analysis: Applied to Ribo-seq data from PC3 human prostate cancer cells with and without PP242 treatment to study translation regulation at the isoform level.
- Isoform- and codon-level translation analysis: Revealed distinct translational efficiency and regulatory patterns among isoforms of genes involved in cell invasion and metastasis affected by PP242, with CRI indicating consistent codon-level translational patterns.
Methodology:
Uses a deep learning model to assign multi-mapped Ribo-seq reads and to estimate isoform-level ribosome abundance and profiles without RNA-seq; computes the Codon Residence Index (CRI) to quantify relative ribosome traversal speed across synonymous codons.
Topics
Details
- Tool Type:
- command-line tool
- Programming Languages:
- Python
- Added:
- 1/14/2020
- Last Updated:
- 12/20/2020
Operations
Publications
Cui H, Hu H, Zeng J, Chen T. DeepShape: estimating isoform-level ribosome abundance and distribution with Ribo-seq data. BMC Bioinformatics. 2019;20(S24). doi:10.1186/s12859-019-3244-0. PMID:31861979. PMCID:PMC6923924.
Links
Issue tracker
https://github.com/cuihf06/DeepShape/issues