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Assessing NGS-based computational methods for predicting transcriptional regulators with query gene sets
Biorxiv : the Preprint Server for Biology
|April 2, 2024
Summary
This review evaluates computational methods for predicting transcriptional regulators (TRs) using next-generation sequencing (NGS) data. BART, ChIP-Atlas, and Lisa show superior performance in identifying TRs from gene sets.
Area of Science:
- Bioinformatics
- Computational Biology
- Genomics
Background:
- Accurate identification of transcriptional regulators (TRs) is crucial for understanding biological development, disease mechanisms, and therapeutic target prediction.
- Numerous computational methods utilizing next-generation sequencing (NGS) data exist, but a systematic evaluation is lacking.
Approach:
- Classified NGS-based TR prediction methods into library-based and region-based categories.
- Conducted benchmark studies evaluating accuracy, sensitivity, coverage, and usability of these methods using molecular experimental datasets.
- Compared NGS-based methods against traditional motif-based approaches.
Key Points:
- NGS-based methods generally outperform motif-based methods for TR prediction.
- Region-centric NGS methods utilizing larger databases exhibit better performance.
- BART, ChIP-Atlas, and Lisa are recommended for their strong performance across various scenarios.
Conclusions:
- Identified limitations of current NGS-based TR prediction tools.
- Highlighted potential areas for future improvements in computational TR identification methods.
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