Enhancing RNA-seq analysis by addressing all co-existing biases using a self-benchmarking approach with 2D structural insights

We introduce a groundbreaking approach: the minimum free energy-based Gaussian Self-Benchmarking (MFE-GSB) framework, designed to combat the myriad of biases inherent in RNA-seq data. Central to our methodology is the MFE concept, facilitating the adoption of a Gaussian distribution model tailored to effectively mitigate all co-existing biases within a k-mer counting scheme. The MFE-GSB framework operates on a sophisticated dual-model system, juxtaposing modeling data of uniform k-mer distribution against the real, observed sequencing data characterized by nonuniform k-mer distributions. The framework applies a Gaussian function, guided by the predetermined parameters-mean and SD-derived from modeling data, to fit unknown sequencing data. This dual comparison allows for the accurate prediction of k-mer abundances across MFE categories, enabling simultaneous correction of biases at the single k-mer level. Through validation with both engineered RNA constructs and human tissue RNA samples, its wide-ranging efficacy and applicability are demonstrated.

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Publication Details

Journal
Briefings in Bioinformatics
Published
2024-09-23
DOI
https://doi.org/10.1093/bib/bbae532
Primary Topic
Cancer-related molecular mechanisms research
Type
article
Field-Weighted Citation Impact
0.00

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article

Enhancing RNA-seq analysis by addressing all co-existing biases using a self-benchmarking approach with 2D structural insights

Deming Gou, Qizhou Lian, Qiang Su, Junmin Quan et al.
Briefings in Bioinformatics
Cancer-related molecular mechanisms research
article

Enhancing RNA-seq analysis by addressing all co-existing biases using a self-benchmarking approach with 2D structural insights

Deming Gou, Qizhou Lian, Qiang Su, Junmin Quan, Yi Long
article en

Abstract

We introduce a groundbreaking approach: the minimum free energy-based Gaussian Self-Benchmarking (MFE-GSB) framework, designed to combat the myriad of biases inherent in RNA-seq data. Central to our methodology is the MFE concept, facilitating the adoption of a Gaussian distribution model tailored to effectively mitigate all co-existing biases within a k-mer counting scheme. The MFE-GSB framework operates on a sophisticated dual-model system, juxtaposing modeling data of uniform k-mer distribution against the real, observed sequencing data characterized by nonuniform k-mer distributions. The framework applies a Gaussian function, guided by the predetermined parameters-mean and SD-derived from modeling data, to fit unknown sequencing data. This dual comparison allows for the accurate prediction of k-mer abundances across MFE categories, enabling simultaneous correction of biases at the single k-mer level. Through validation with both engineered RNA constructs and human tissue RNA samples, its wide-ranging efficacy and applicability are demonstrated.

Briefings in BioinformaticsVol. 25(6)
Shenzhen University (CN), Peking University (CN), Shenzhen Bay Laboratory (CN), Guangzhou Women and Children Medical Center (CN), Shenzhen Institutes of Advanced Technology (CN), State Key Laboratory of Pharmaceutical Biotechnology, University of Hong Kong (HK), Guangzhou Medical University (CN)
National Natural Science Foundation of China, National Key Research and Development Program of China
Affordable and clean energy
Openalex Percentile: Top 73%
Cancer-related molecular mechanisms research
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Enhancing RNA-seq analysis by addressing all co-existing biases using a self-benchmarking approach with 2D structural insights — Deming Gou, Qizhou Lian, et al. · Briefings in Bioinformatics (2024) | TGRS Research Map | TGRS