Trendy

Trendy identifies and characterizes dynamic changes in gene expression from high-throughput ordered-condition experiments such as time-course and spatial-course studies.


Key Features:

  • Segmented Regression Models: Employs segmented (breakpoint) regression models to estimate breakpoints that indicate changes in gene expression levels.
  • Gene-Specific Expression Patterns: Selects an optimal segmented regression model for each gene to locate breakpoint positions and determine the direction of expression changes.
  • Global Dynamic Activity Summarization: Summarizes dynamic activity across the transcriptome to highlight critical time points or spatial locations with coordinated expression changes.
  • Data Type Support: Applies to high-throughput expression data including microarray and RNA-seq datasets.
  • Ordered-Condition Analysis: Targets experiments with ordered conditions (e.g., time-course, spatial-course) to detect temporal or spatial expression dynamics.

Scientific Applications:

  • Differentiation and developmental studies: Identifies timing and sequence of gene expression changes during differentiation processes.
  • Spatial patterning analysis: Detects location-specific expression dynamics underlying spatial patterning.
  • Identification of critical time points and pathways: Highlights critical time points and coordinated transcriptome changes relevant to biological pathways and cellular behaviors.

Methodology:

Uses segmented (breakpoint) regression models to estimate breakpoints, selects optimal segmented regression models per gene, and summarizes global dynamic activity across the transcriptome.

Topics

Collections

Details

License:
GPL-3.0
Tool Type:
library
Operating Systems:
Linux, Windows, Mac
Programming Languages:
R
Added:
7/15/2018
Last Updated:
12/10/2018

Operations

Publications

Bacher R, Leng N, Chu L, Thomson J, Kendziorski C, Stewart R. Trendy: Segmented regression analysis of expression dynamics for high-throughput ordered profiling experiments. Unknown Journal. 2017. doi:10.1101/185413.

Documentation

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