Piphillin

Piphillin infers microbial community gene composition and functional capacity directly from 16S rRNA gene profiles using a non-phylogenetic, database-driven approach for metagenomic functional prediction.


Key Features:

  • Independence from Phylogenetic Trees: Does not rely on phylogenetic tree structures for functional inference.
  • Direct Inference Approach: Performs direct inference of gene content from 16S rRNA gene profiles rather than indirect, phylogeny-based imputation.
  • Utilization of Contemporary Functional Databases: Leverages up-to-date functional databases to map sequence data to inferred gene compositions.
  • No Specific Data Pre-processing Protocols Required: Operates without requiring specific data pre-processing protocols.

Scientific Applications:

  • Human clinical samples functional prediction: Predicts the functional capacity of microbial communities within human clinical samples and was evaluated against shotgun metagenomics data.
  • Performance against other tools: Outperformed PICRUSt (p<0.01) and Tax4Fun (p<0.001) in comparisons to shotgun metagenomics.
  • Disease association prediction: Demonstrated a 15% increase in balanced accuracy for predicting disease associations with specific gene orthologs compared to PICRUSt.
  • Laboratory animal and environmental samples: Showed no significant performance difference from other tools on laboratory animal and environmental samples, with environmental predictions generally unsatisfactory across methods.

Methodology:

Piphillin uses a direct inference approach that does not rely on phylogenetic trees, leverages contemporary functional databases, and infers functional gene composition from 16S rRNA gene profiles without requiring specific data pre-processing protocols.

Topics

Details

Tool Type:
web application
Operating Systems:
Linux, Windows, Mac
Added:
5/29/2018
Last Updated:
12/10/2018

Operations

Publications

Iwai S, Weinmaier T, Schmidt BL, Albertson DG, Poloso NJ, Dabbagh K, DeSantis TZ. Piphillin: Improved Prediction of Metagenomic Content by Direct Inference from Human Microbiomes. PLOS ONE. 2016;11(11):e0166104. doi:10.1371/journal.pone.0166104. PMID:27820856. PMCID:PMC5098786.

PMID: 27820856
PMCID: PMC5098786
Funding: - National Cancer Institute: R01 CA131286, R21 CA163019 - National Institute of Dental and Craniofacial Research: R01 DE019796 - National Center for Advancing Translational Sciences: UL1 RR024129

Documentation