Evidence map›Paper›PMID 39428128›Full record

ArticleBriefings in bioinformatics2024

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

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

Abstract read
In one paragraph

Article in Briefings in bioinformatics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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.

2 · The registry

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.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Qiang SuFaculty of Synthetic Biology, Shenzhen University of Advanced Technology, Shenzhen Key Laboratory of Quantitative Synthetic Biology, Shenzhen Institute of Synthetic Biology, Shenzhen Institutes of Advanced Technology, Chinese Academy of Sciences, 1068 Xueyuan Avenue, Nanshan District, Shenzhen, 518055, China.ORCID 0000-0001-7922-8996
Yi LongInstitute of Chemical Biology, Shenzhen Bay Laboratory, Gaoke International Innovation Center A14, Guangqiao Road, Guangming District, Shenzhen, 518132, China.
Deming GouShenzhen Key Laboratory of Microbial Genetic Engineering, Vascular Disease Research Center, College of Life Sciences and Oceanography, Shenzhen University, 1066 Xueyuan Street, Nanshan District, Shenzhen, 518055, China.
Junmin QuanState Key Laboratory of Chemical Oncogenomics, School of Chemical Biology and Biotechnology, Peking University Shenzhen Graduate School, 2199 Lishui Avenue, Nanshan District, Shenzhen, 518055, China.
Qizhou LianFaculty of Synthetic Biology, Shenzhen University of Advanced Technology, Shenzhen Key Laboratory of Quantitative Synthetic Biology, Shenzhen Institute of Synthetic Biology, Shenzhen Institutes of Advanced Technology, Chinese Academy of Sciences, 1068 Xueyuan Avenue, Nanshan District, Shenzhen, 518055, China.

Funding

Guangdong Provincial Key Laboratory of Regional Immunity and Diseases 2019B030301009Long Yi Postdoctoral Special Fund S249201002National Key Research and Development Program of China 2022YFA1105601National Natural Science Foundation of China 82241022Shenzhen-Hong Kong Collaborative Innovation ResearchShenzhen Municipal Research Grant JCYJ20210324120206017Yunnan Provincial People's Hospital Cooperation Project 202201AY070001-224
6 · The paper itself

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.

Indexed as

RNA-SeqAlgorithmsBenchmarkingBiasComputational BiologyHumansNormal DistributionRNASequence Analysis, RNARNAGaussian distributionk-merMFE-GSBRNA-seq

Identifiers

PMID39428128
PMCPMC11491153

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Registered trials

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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.