Evidence map›Paper›PMID 40501932›Full record

ArticlebioRxiv : the preprint server for biology2025

Comparing phenotypic manifolds with Kompot: Detecting differential abundance and gene expression at single-cell resolution.

Dominik J Otto, Erica Arriaga-Gomez, Elana Thieme, Ruijin Yang, Stanley C Lee, Manu Setty

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Dominik J OttoBasic Sciences Division, Fred Hutchinson Cancer Center, Seattle WA.ORCID 0000-0002-6116-053X
Erica Arriaga-GomezTranslational Science and Therapeutics Division, Fred Hutchinson Cancer Center, Seattle WA.ORCID 0000-0002-8237-6751
Elana ThiemeBasic Sciences Division, Fred Hutchinson Cancer Center, Seattle WA.ORCID 0000-0002-6012-1117
Ruijin YangBasic Sciences Division, Fred Hutchinson Cancer Center, Seattle WA.ORCID 0009-0001-3813-4747
Stanley C LeeTranslational Science and Therapeutics Division, Fred Hutchinson Cancer Center, Seattle WA.ORCID 0000-0001-7110-2416
Manu SettyBasic Sciences Division, Fred Hutchinson Cancer Center, Seattle WA.ORCID 0000-0002-0344-2627

Funding

Training in Cellular & Molecular BiologyT32GM136534 · NIGMS · UNIVERSITY OF WASHINGTON · PI Andrew Atwell Oberst, LARRY S ZWEIFEL · 2021 to 2026
$5.8M
Causes and consequences of genomic instability in myelodysplasiaR01CA292932 · NCI · FRED HUTCHINSON CANCER CENTER · PI Stanley Chun-Wei Lee · 2024 to 2026
$2.7M
Computational Modeling of Lineage Decisions using Single-cell DataR35GM147125 · NIGMS · FRED HUTCHINSON CANCER CENTER · PI Manu N Setty · 2022 to 2026
$2.1M
High-Performance Compute Cluster for Comprehensive Cancer and Infectious Diseases ResearchS10OD028685 · OD · FRED HUTCHINSON CANCER RESEARCH CENTER · PI BRADLEY, PHILIP · 2020 to 2020
$2.0M
NCI NIH HHS R01 CA292932NIGMS NIH HHS R35 GM147125NIGMS NIH HHS T32 GM136534NIH HHS S10 OD028685
6 · The paper itself

Abstract

Kompot is a statistical framework for holistic comparison of multi-condition single-cell datasets, supporting both differential abundance and differential expression. Differential abundance captures changes in how cells populate the phenotypic manifold across conditions, while differential expression identifies condition-specific changes in gene regulation that may be localized to particular regions of that manifold. Kompot models the distribution of cells and gene expression as continuous functions over a low-dimensional representation of cell states, enabling single-cell resolution inference with calibrated uncertainty estimates. Applying Kompot to aging murine bone marrow, we identified a continuum of shifts in hematopoietic stem cell and mature cell states, transcriptional remodeling of monocytes independent of compositional changes, and divergent regulation of oxidative stress response genes across cell types. By capturing both global and cell-state-specific effects of perturbation, Kompot reveals how aging reshapes cellular identity and regulatory programs across the hematopoietic landscape. This framework is broadly applicable to dissecting condition-specific effects in complex single-cell landscapes.

Identifiers

PMID40501932
PMCPMC12157388

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Registered trials

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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.