Evidence map›Paper›PMID 37398158›Full record

ArticlebioRxiv : the preprint server for biology2023

Unbiased single-cell morphology with self-supervised vision transformers.

Michael Doron, Théo Moutakanni, Zitong S Chen, Nikita Moshkov, Mathilde Caron, Hugo Touvron, Piotr Bojanowski, Wolfgang M Pernice, Juan C Caicedo

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2023. 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

9 authors.

Michael DoronBroad Institute of MIT and Harvard, Cambridge, MA, USA.
Théo MoutakanniMeta AI, Paris, France.
Zitong S ChenBroad Institute of MIT and Harvard, Cambridge, MA, USA.
Nikita MoshkovSynthetic and Systems Biology Unit, Biological Research Centre (BRC), Szeged, Hungary.
Mathilde CaronMeta AI, Paris, France.
Hugo TouvronMeta AI, Paris, France.
Piotr BojanowskiMeta AI, Paris, France.
Wolfgang M PerniceDepartment of Neurology, Columbia University Medical Center, New York, NY, USA.
Juan C CaicedoBroad Institute of MIT and Harvard, Cambridge, MA, USA.

Funding

Integrated morphological and transcriptomic single-cell profiling of patient-derived cells as a platform for genomic and translational medicineR00HG011488 · NHGRI · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI PERNICE, WOLFGANG MAXIMILIAN ANTON · 2023 to 2025
$726k
Deep-learning based profiling of patient-derived cells as a tool for genomic and translational medicineK99HG011488 · NHGRI · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI PERNICE, WOLFGANG MAXIMILIAN ANTON · 2021 to 2022
$196k
NHGRI NIH HHS K99 HG011488NHGRI NIH HHS R00 HG011488
6 · The paper itself

Abstract

Accurately quantifying cellular morphology at scale could substantially empower existing single-cell approaches. However, measuring cell morphology remains an active field of research, which has inspired multiple computer vision algorithms over the years. Here, we show that DINO, a vision-transformer based, self-supervised algorithm, has a remarkable ability for learning rich representations of cellular morphology without manual annotations or any other type of supervision. We evaluate DINO on a wide variety of tasks across three publicly available imaging datasets of diverse specifications and biological focus. We find that DINO encodes meaningful features of cellular morphology at multiple scales, from subcellular and single-cell resolution, to multi-cellular and aggregated experimental groups. Importantly, DINO successfully uncovers a hierarchy of biological and technical factors of variation in imaging datasets. The results show that DINO can support the study of unknown biological variation, including single-cell heterogeneity and relationships between samples, making it an excellent tool for image-based biological discovery.

Identifiers

PMID37398158
PMCPMC10312751

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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.