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This document describes the BABAR R package, which automates the loading and normalisation of two-colour, common reference design microarrays for transcriptomic datasets. It includes installation
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How to fill out BABAR: an R package to simplify the normalisation of common reference design microarray-based transcriptomic datasets

01
Install the BABAR package from CRAN using the command: install.packages('BABAR')
02
Load the BABAR library into your R session with: library(BABAR)
03
Prepare your input data in the format required by the package, which typically includes a matrix of expression values.
04
Specify the reference samples you will use for normalization based on your experimental design.
05
Use the normalization function provided by BABAR, passing your data and reference samples as arguments.
06
Examine the output of the normalization process, which should include normalized expression values.
07
Optionally, you can visualize the results to assess the quality of normalization using the built-in plotting functions.

Who needs BABAR: an R package to simplify the normalisation of common reference design microarray-based transcriptomic datasets?

01
Researchers and bioinformaticians dealing with microarray-based transcriptomic datasets.
02
Scientists looking for efficient ways to normalize data from common reference design experiments.
03
Users of microarray technologies who need reproducible normalization methods to compare gene expression levels across samples.
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BABAR is an R package designed to streamline the process of normalizing microarray-based transcriptomic datasets that use a common reference design.
Researchers and scientists who work with microarray-based transcriptomic data and are looking to normalize their datasets using a common reference design are required to file BABAR.
To fill out BABAR, users typically need to input their raw data, specify the common reference design, and select normalization parameters that fit their dataset before running the normalization process.
The purpose of BABAR is to facilitate the normalization of transcriptomic datasets, allowing for better comparison and analysis of gene expression across different samples.
Users must report the input dataset, normalization settings, parameters chosen for analysis, and any relevant metadata associated with the transcriptomic data.
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