MSProGene

MSProGene generates sample-specific transcripts from RNA-Seq and integrates RNA-Seq with peptide evidence to construct a proteogenomic network optimized by a maximum-flow algorithm for resolving shared-peptide ambiguity and improving gene and protein predictions.


Key Features:

  • Customized Transcript Databases: Generates sample-specific transcripts directly from RNA-Seq, avoiding large six-frame translated databases and reducing computational complexity while enhancing proteomic specificity.
  • Database Independence: Operates without reliance on existing reference databases or annotated SNPs, enabling analyses that do not depend on prior annotations.
  • Integration of Multi-Omics Data: Combines RNA-Seq and peptide information to construct a proteogenomic network optimized using a maximum-flow algorithm to address shared peptide ambiguity in protein inference.
  • Novel Gene Identification: Supports identification of novel genes, facilitating discovery in unannotated organisms.

Scientific Applications:

  • Proteogenomics: Enables sample-specific proteogenomic analyses by integrating transcriptomic and peptide evidence to improve protein inference.
  • Protein and Gene Prediction: Improves accuracy of gene and protein predictions by resolving shared-peptide ambiguity through network optimization.
  • Novel Gene Discovery in Unannotated Organisms: Facilitates detection of novel genes in organisms lacking comprehensive annotations.

Methodology:

Generates sample-specific transcripts from RNA-Seq; combines RNA-Seq and peptide information into a proteogenomic network; optimizes that network using a maximum-flow algorithm; operates independently of reference databases and annotated SNPs and avoids six-frame translated databases.

Topics

Collections

Details

Tool Type:
command-line tool
Operating Systems:
Linux, Windows, Mac
Programming Languages:
Java
Added:
8/3/2017
Last Updated:
11/25/2024

Operations

Publications

Zickmann F, Renard BY. MSProGene: integrative proteogenomics beyond six-frames and single nucleotide polymorphisms. Bioinformatics. 2015;31(12):i106-i115. doi:10.1093/bioinformatics/btv236. PMID:26072472. PMCID:PMC4765881.

Documentation

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