Evidence map›Paper›PMID 40234751›Full record

ArticleBMC bioinformatics2025

Redefining the high variable genes by optimized LOESS regression with positive ratio.

Yue Xie, Zehua Jing, Hailin Pan, Xun Xu, Qi Fang

Abstract read
In one paragraph

Article in BMC bioinformatics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

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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.

Yue Xie *College of Life Sciences, University of Chinese Academy of Sciences, Beijing, 100049, China.
Zehua Jing *College of Life Sciences, University of Chinese Academy of Sciences, Beijing, 100049, China.
Hailin PanBGI Research, Shenzhen, 518083, China.
Xun XuCollege of Life Sciences, University of Chinese Academy of Sciences, Beijing, 100049, China. xuxun@genomics.cn.
Qi FangBGI Research, Shenzhen, 518083, China. fangqi@genomics.cn.

Funding

Guangdong Provincial Key Laboratory of Genome Read and Write 2017B030301011National Key Research and Development Program of China 2022YFC3400400
6 · The paper itself

Abstract

backgroundSingle-cell RNA sequencing allows for the exploration of transcriptomic features at the individual cell level, but the high dimensionality and sparsity of the data pose substantial challenges for downstream analysis. Feature selection, therefore, is a critical step to reduce dimensionality and enhance interpretability.

resultsWe developed a robust feature selection algorithm that leverages optimized locally estimated scatterplot smoothing regression (LOESS) to precisely capture the relationship between gene average expression level and positive ratio while minimizing overfitting. Our evaluations showed that our algorithm consistently outperforms eight leading feature selection methods across three benchmark criteria and helps improve downstream analysis, thus offering a significant improvement in gene subset selection.

conclusionsBy preserving key biological information through feature selection, GLP provides informative features to enhance the accuracy and effectiveness of downstream analyses.

Indexed as

AlgorithmsComputational BiologyGene Expression ProfilingSequence Analysis, RNASingle-Cell AnalysisHumansRegression AnalysisTranscriptomeFeature selectionHigh variable genesSingle cell transcriptome

Identifiers

PMID40234751
PMCPMC12001687

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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.