Evidence map›Paper›PMID 40391084›Full record

ArticleNAR genomics and bioinformatics2025

Ocelli: an open-source tool for the analysis and visualization of developmental multimodal single-cell data.

Piotr Rutkowski, Marcin Tabaka

Abstract read
In one paragraph

Article in NAR genomics and bioinformatics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

2 authors.

Piotr RutkowskiInternational Centre for Translational Eye Research, Skierniewicka 10A, Warsaw 01-230, Poland.ORCID https://orcid.org/0000-0001-8009-0816
Marcin TabakaInternational Centre for Translational Eye Research, Skierniewicka 10A, Warsaw 01-230, Poland.ORCID https://orcid.org/0000-0002-6166-2820

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The recent expansion of single-cell technologies has enabled simultaneous genome-wide measurements of multiple modalities in the same single cell. The potential to jointly profile such modalities as gene expression, chromatin accessibility, protein epitopes, or multiple histone modifications at single-cell resolution represents a compelling opportunity to study developmental processes at multiple layers of gene regulation. Here, we present Ocelli, a lightweight Python package implemented in Ray for scalable visualization and analysis of developmental multimodal single-cell data. The core functionality of Ocelli focuses on diffusion-based modeling of biological processes involving cell state transitions. Ocelli addresses common tasks in single-cell data analysis, such as visualization of cells on a low-dimensional embedding that preserves the continuity of the developmental progression of cells, identification of rare and transient cell states, integration with trajectory inference algorithms, and imputation of undetected feature counts. Extensive benchmarking shows that Ocelli outperforms existing methods regarding computational time and quality of the reconstructed low-dimensional representation of developmental data.

Indexed as

Single-Cell AnalysisSoftwareAlgorithmsAnimalsHumans

Identifiers

PMID40391084
PMCPMC12086682

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.