Evidence map›Paper›PMID 40225837›Full record

ArticleComputational and structural biotechnology journal2025

The impact of dropouts in scRNAseq dense neighborhood analysis.

Alisa Pavel, Manja Gersholm Grønberg, Line H Clemmensen

Abstract read
In one paragraph

Article in Computational and structural biotechnology journal, 2025. 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

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2 · The registry

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3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

  1. Article
  2. Pathway Analysis Interpretation in the Multi-Omic Era.Biotech (Basel (Switzerland)) · 2025
    Review
  3. Article
  4. Article
4 · The record

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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

3 authors.

Alisa PavelDepartment of Applied Mathematics and Computer Science, Technical University of Denmark, 2800, Kongens Lyngby, Denmark.
Manja Gersholm GrønbergDepartment of Applied Mathematics and Computer Science, Technical University of Denmark, 2800, Kongens Lyngby, Denmark.
Line H ClemmensenDepartment of Applied Mathematics and Computer Science, Technical University of Denmark, 2800, Kongens Lyngby, Denmark.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Single cell RNA sequencing (scRNAseq) provides the possibility to investigate transcriptomic profiles on a single cell level. However, the data show unique challenges in comparison to bulk transcriptomic data, one being high dropout rates, which yields high sparsity data. Many classical analysis and preprocessing pipelines are based on the assumption that poor data can be counteracted by quantity and that similar cells (samples) are close to each other in space. Clustering is commonly used to detect clusters (dense local cell neighborhoods) under the assumption that similar cells are close to each other in space (where close is dependent on the (distance) metric used). The most commonly used clustering methodologies to detect dense local neighborhoods are based on graph clustering on a nearest neighbor graph. However, high dropout rates may break this assumption and make it difficult to reliably detect such dense local neighborhoods. We assess the cluster homogeneity and stability under increasing degrees of dropouts in one of the most popular clustering pipelines (dimensionality reduction + graph based clustering), as provided by scRNAseq analyses packages Seurat and Scanpy. Our study showcases that while the default pipeline performs well in terms of cluster homogeneity (i.e., cells in a cluster are of the same type), also with increasing dropout rates, the stability of clusters (i.e., cell pairs consistently being in the same cluster) decreases. This implies that sub-populations within cell types are increasingly difficult to identify under increasing dropout rates because observations are not consistently close. Our results challenge the current practice of using default clustering pipelines and the general assumption of identifiable local neighborhoods on high dropout data. Hence, these results suggest that careful consideration in interpretation and downstream analysis need to be made when relying on local neighborhoods and clusters on scRNAseq data. In addition, these results call for extensive benchmarking, to identify and provide methods robust in their local neighborhood relationships on data containing low to high dropout rates.

Indexed as

ClusteringDropoutsscRNAseqSparsity

Identifiers

PMID40225837
PMCPMC11992407

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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.