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Mapping the Structure-Function Relationships of Disordered Oncogenic Transcription Factors Using Transcriptomic Analysis
Published on: June 27, 2020
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Investigation of normalization procedures for transcriptome profiles of compounds oriented toward practical study
Tadahaya Mizuno1, Hiroyuki Kusuhara1
1Laboratory of Molecular Pharmacokinetics, Graduate School of Pharmaceutical Sciences, The University of Tokyo.
The Journal of Toxicological Sciences
|June 2, 2024
Summary
This study optimizes transcriptome profiling for compound effects by evaluating normalization methods. It finds that using all samples within a batch for baseline distribution improves robustness, especially for small datasets.
Area of Science:
- Transcriptomics
- Computational Biology
- Pharmacogenomics
Background:
- Transcriptome profiles are key for understanding compound effects.
- Batch effects are a common challenge in high-throughput data.
- Existing methods often require large sample sizes, limiting small dataset applications.
Purpose of the Study:
- To investigate normalization procedures for robust transcriptome-based compound profiles.
- To address challenges in small dataset scenarios.
- To determine optimal baseline distributions and control sample quantities.
Main Methods:
- Evaluated normalization procedures on two large GeneChip datasets.
- Assessed profile similarity between replicates and across datasets.
- Conducted simulations to explore control sample size impact.
Main Results:
- Using all samples within a batch (batch-corrected) as the baseline distribution is effective for large datasets.
- Identified insights into the optimal number of control samples for small datasets.
- Demonstrated the impact of normalization on profile robustness.
Conclusions:
- Recommends specific normalization strategies for transcriptome profiling.
- Provides guidance on designing transcriptome analyses for small datasets.
- Enhances understanding for practical application of compound transcriptome profiles.
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