ArticleBriefings in bioinformatics2025
Machine learning-augmented m6A-Seq analysis without a reference genome.
Article in Briefings in bioinformatics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
1 citing paper in PubMed.
- Review
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
9 authors.
Funding
Abstract
Methylated RNA m6A immunoprecipitation sequencing (m6A-Seq) is a powerful technique for investigating transcriptome-wide m6A modification. However, most of the existing m6A-Seq protocols rely on reference genomes, limiting their use in species lacking sequenced genomes. Here, we introduce mlPEA, a user-friendly, multi-functional platform specifically tailored to the streamlined processing of m6A-Seq data in a reference genome-free manner. mlPEA provides a comprehensive collection of functions required for performing transcriptome-wide m6A identification and analysis, where the reference-de novo assembled transcriptome-is built solely using m6A-Seq data. By taking advantage of machine learning (ML) algorithms, mlPEA enhances m6A-Seq data analysis by constructing robust computational models for identifying high-quality transcripts and high-confidence m6A-modified regions. These functions and ML models have been integrated into a web-based Galaxy framework. This ensures that mlPEA has powerful data interaction and visualization capabilities, with flexibility, traceability, and reproducibility throughout the analytical process. mlPEA also has high compatibility and portability as it employs advanced packaging technology, dramatically simplifying its large-scale application in various species. Validated through case studies of Arabidopsis, maize, and wheat, mlPEA has demonstrated its utility and robustness regarding reference genome-free m6A-Seq data analysis for plants of various genomic complexities. mlPEA is freely available via GitHub: https://github.com/cma2015/mlPEA.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.