Evidence map›Paper›PMID 38678050›Full record

ArticleNature communications2024

scLENS: data-driven signal detection for unbiased scRNA-seq data analysis.

Hyun Kim, Won Chang, Seok Joo Chae, Jong-Eun Park, Minseok Seo, Jae Kyoung Kim

Abstract read
In one paragraph

Article in Nature communications, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Principled PCA separates signal from noise in omics count data.bioRxiv : the preprint server for biology · 2025
    Article
  4. 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

6 authors.

Hyun KimBiomedical Mathematics Group, Pioneer Research Center for Mathematical and Computational Sciences, Institute for Basic Science, Daejeon, 34126, Republic of Korea.
Won ChangDivision of Statistics and Data Science, University of Cincinnati, Cincinnati, OH, 45221, USA.ORCID http://orcid.org/0000-0003-3556-1249
Seok Joo ChaeBiomedical Mathematics Group, Pioneer Research Center for Mathematical and Computational Sciences, Institute for Basic Science, Daejeon, 34126, Republic of Korea.
Jong-Eun ParkGraduate School of Medical Science and Engineering, KAIST, Daejeon, 34141, Republic of Korea.ORCID http://orcid.org/0000-0002-1687-2423
Minseok SeoDepartment of Computer and Information Science, Korea University, Sejong, 30019, Republic of Korea.
Jae Kyoung KimBiomedical Mathematics Group, Pioneer Research Center for Mathematical and Computational Sciences, Institute for Basic Science, Daejeon, 34126, Republic of Korea. jaekkim@kaist.ac.kr.ORCID http://orcid.org/0000-0001-7842-2172

Funding

Institute for Basic Science (IBS) R029-C3National Research Foundation of Korea (NRF) 2021R1A5A8032895UC | Charles Phelps Taft Research Center (Taft Research Center) M80941
6 · The paper itself

Abstract

High dimensionality and noise have limited the new biological insights that can be discovered in scRNA-seq data. While dimensionality reduction tools have been developed to extract biological signals from the data, they often require manual determination of signal dimension, introducing user bias. Furthermore, a common data preprocessing method, log normalization, can unintentionally distort signals in the data. Here, we develop scLENS, a dimensionality reduction tool that circumvents the long-standing issues of signal distortion and manual input. Specifically, we identify the primary cause of signal distortion during log normalization and effectively address it by uniformizing cell vector lengths with L2 normalization. Furthermore, we utilize random matrix theory-based noise filtering and a signal robustness test to enable data-driven determination of the threshold for signal dimensions. Our method outperforms 11 widely used dimensionality reduction tools and performs particularly well for challenging scRNA-seq datasets with high sparsity and variability. To facilitate the use of scLENS, we provide a user-friendly package that automates accurate signal detection of scRNA-seq data without manual time-consuming tuning.

Indexed as

AlgorithmsRNA-SeqSingle-Cell Gene Expression AnalysisAnimalsComputational BiologyData AnalysisHumansRNA, Small CytoplasmicSoftwareRNA, Small Cytoplasmic

Identifiers

PMID38678050
PMCPMC11519519

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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.