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