Evidence map›Paper›PMID 41330382›Full record

ArticleCell genomics2026

CellUntangler: Separating distinct biological signals in single-cell data with deep generative models.

Sarah Chen, Aviv Regev, Anne Condon, Jiarui Ding

Abstract read
In one paragraph

Article in Cell genomics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. 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

4 authors.

Sarah ChenDepartment of Computer Science, University of British Columbia, Vancouver, BC V6T 1Z4, Canada.
Aviv RegevBroad Institute of MIT and Harvard, Cambridge, MA, USA.
Anne CondonDepartment of Computer Science, University of British Columbia, Vancouver, BC V6T 1Z4, Canada.
Jiarui DingDepartment of Computer Science, University of British Columbia, Vancouver, BC V6T 1Z4, Canada. Electronic address: jiarui.ding@ubc.ca.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Single-cell RNA sequencing has provided new insights into both intracellular and intercellular processes. However, multiple processes, such as cell-type programs, differentiation, and the cell cycle, often occur simultaneously within one cell. Existing methods typically target a single process and impose restrictive assumptions, risking the loss of valuable biological information. We introduce CellUntangler, a deep generative model that embeds cells into a latent space composed of multiple subspaces, each tailored with an appropriate geometry to capture a distinct signal. Applied to datasets of cycling-only and mixed cycling/non-cycling cells, CellUntangler disentangles the cell cycle from other processes such as cell type. The framework generalizes to disentangle additional signals, including spatial, tissue dissociation, interferon response, and cell-type identity. By providing flexible embeddings to capture various signals, CellUntangler enables selective enhancement or filtering of signals at the gene-expression level, offering a powerful tool for disentangling complex biological processes in single-cell data.

Indexed as

Sequence Analysis, RNASingle-Cell AnalysisAlgorithmsCell CycleHumansSignal Transductioncell cycledeep generative modelshyperbolic spacenon-Euclidean spaceperturbationpseudospacesingle-cell RNA sequencingspatiotemporalvariational autoencoder

Identifiers

PMID41330382
PMCPMC12903416

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.