BRIC-seq is a genome-wide approach for determining RNA stalibity in mammalian cells. bridger2
provides a series of functions for performing a comprehensive BRIC-seq data analysis. After estimating the RPKM values for all genes from your BRIC-seq fastq files, you can easily analyze your BRIC-seq data using bridger2 R package.
To make that happen, bridger2
:
* Checks the quality of your BRIC-seq data.
Normalizes RPKM values of your BRIC-seq data.
Calculates RNA half-life for each transcript
Compares RNA half-lives between two conditions.
Displays RNA decay curve using a web browser (powered by shiny).
# The the development version from GitHub:
# install.packages("devtools")
devtools::install_github("Imamachi-n/BridgeR2")
Here I show the most basic step for analyzing your BRIC-seq data. This step require matrix
object (named RNA_halflife_comparison
in this case) of the RPKM values from your BRIC-seq data. BridgeRCore
function returns data.table
object including RNA half-life, R2 and the selected fitting model.
halflife_table <- BridgeRCore(RNA_halflife_comparison)
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