Evidence map›Paper›PMID 41587323›Full record

ReviewBriefings in bioinformatics2026

Unveiling patterns: an exploration of machine learning techniques for unsupervised feature selection in single-cell data.

Nandini Chatterjee, Aleksandr Taraskin, Hridya Divakaran, Natalia Jaeger, Victor Enriquez, Catherine C Hedrick, Ahmad Alimadadi

Abstract readReview
In one paragraph

Review in Briefings in bioinformatics, 2026. 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. Review
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

7 authors.

Nandini ChatterjeeLa Jolla Institute for Immunology, 9420 Athena Cir, La Jolla, CA 92037, United States.
Aleksandr TaraskinImmunology Center of Georgia, Augusta University, 1410 Laney Walker Blvd, Augusta, GA 30912, United States.
Hridya DivakaranImmunology Center of Georgia, Augusta University, 1410 Laney Walker Blvd, Augusta, GA 30912, United States.
Natalia JaegerImmunology Center of Georgia, Augusta University, 1410 Laney Walker Blvd, Augusta, GA 30912, United States.
Victor EnriquezImmunology Center of Georgia, Augusta University, 1410 Laney Walker Blvd, Augusta, GA 30912, United States.
Catherine C HedrickImmunology Center of Georgia, Augusta University, 1410 Laney Walker Blvd, Augusta, GA 30912, United States.
Ahmad AlimadadiLa Jolla Institute for Immunology, 9420 Athena Cir, La Jolla, CA 92037, United States.ORCID 0000-0002-7888-5019

Funding

Project 4: APOB-specific CD4 and CD8 T cells exacerbate atherosclerosisP01HL136275 · NHLBI · LA JOLLA INSTITUTE FOR IMMUNOLOGY · PI Catherine C Hedrick · 2017 to 2026
$25.5M
Neutrophil Survival and Demise During Inflammatory StatesP01HL152958 · NHLBI · SCRIPPS RESEARCH INSTITUTE, THE · PI HOFFMAN, HAROLD M · 2021 to 2025
$12.4M
NHLBI NIH HHS P01 HL136275NHLBI NIH HHS P01 HL152958NIH HHS P01 HL136275NIH HHS P01 HL152958
6 · The paper itself

Abstract

The rapid evolution of single-cell technologies has generated vast, multimodal datasets encompassing genomic, transcriptomic, proteomic, and spatial information. However, high dimensionality, noise, and computational costs pose significant challenges, often introducing bias through traditional feature selection methods, such as highly variable gene selection. Unsupervised machine learning (ML) provides a solution by identifying informative features without predefined labels, thereby minimizing bias and capturing complex patterns. This paper reviews a diverse array of unsupervised ML techniques tailored for single-cell data. These approaches could enhance downstream analyses, such as clustering, dimensionality reduction, visualization, and data denoising, and reveal biologically relevant gene modules. Despite their advantages, challenges such as data sparsity, parameter tuning, and scalability persist. Future directions include integrating multiomic data, incorporating domain-specific knowledge, and developing scalable and interpretable algorithms. By addressing these challenges, unsupervised ML-based feature selection promises to revolutionize single-cell data analysis, driving unbiased insights into cellular heterogeneity and advancing biological discovery.

Indexed as

Computational BiologyMachine LearningSingle-Cell AnalysisUnsupervised Machine LearningAlgorithmsAnimalsClustering AlgorithmsData AnalyticsDimensionality ReductionHumansartificial intelligencebioinformaticsmachine learningpattern recognitionsingle-cell dataunsupervised feature selection

Identifiers

PMID41587323
PMCPMC12834302

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.