Extended Circadian Harmonic Oscillators (ECHO)

Extended Circadian Harmonic Oscillators (ECHO) detects oscillatory patterns in large-scale time-course biological datasets by modeling amplitude changes to characterize circadian, ultradian, and infradian rhythms.


Key Features:

  • Extended Harmonic Oscillator Model: ECHO employs an extended solution of the fixed-amplitude oscillator model that incorporates a coefficient for amplitude change to identify oscillations with varying amplitudes.
  • Performance on synthetic datasets: Evaluations using synthetic datasets show improved detection of rhythms with decreasing amplitudes and accurate recovery of phase shifts.
  • Biological insight into amplitude changes: Identification of rhythms with changing amplitudes in published biological datasets reveals distinct functional subclasses of circadian oscillations and suggests regulatory roles of the circadian clock.
  • Integration with PAICE and R: ECHO is part of the PAICE (Pipeline for Amplitude Integration of Circadian Exploration) Suite and is implemented in R for statistical analysis.

Scientific Applications:

  • Genomic and systems biology: Applies to time-course genomic datasets to identify temporally regulated genes and pathways driven by circadian and other rhythmic processes.
  • Metabolic and pathway analysis: Detects rhythm amplitude changes and phase dynamics relevant to metabolic regulation and pathway-level temporal organization.

Methodology:

Uses an extended harmonic oscillator model with an amplitude-change coefficient; performance assessed on synthetic datasets with recovery of phase shifts; implemented in R and integrated into the PAICE suite.

Topics

Details

License:
MIT
Tool Type:
library
Programming Languages:
R
Added:
11/14/2019
Last Updated:
12/25/2020

Operations

Publications

De los Santos H, Collins EJ, Mann C, Sagan AW, Jankowski MS, Bennett KP, Hurley JM. ECHO: an application for detection and analysis of oscillators identifies metabolic regulation on genome-wide circadian output. Bioinformatics. 2019;36(3):773-781. doi:10.1093/bioinformatics/btz617. PMID:31384918. PMCID:PMC7523678.

PMID: 31384918
Funding: - National Institutes of Health: NIBIB U01 EB022546, NIGMS R35 GM128687, T32GM067545 - Department of Energy: PNNL 47818 - National Science Foundation: #1331023

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