Evidence map›Paper›PMID 33397893›Full record

ArticleNature communications2021

Multi-domain translation between single-cell imaging and sequencing data using autoencoders.

Karren Dai Yang, Anastasiya Belyaeva, Saradha Venkatachalapathy, Karthik Damodaran, Abigail Katcoff, Adityanarayanan Radhakrishnan, G V Shivashankar, Caroline Uhler

Abstract read
In one paragraph

Article in Nature communications, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 95 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
95citing papers in PubMed, 1 pooled it
–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

95 citing papers in PubMed, 1 synthesis or guideline pooled it.

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35 more citing papers are in PubMed but not listed here.

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

8 authors.

Karren Dai YangMassachusetts Institute of Technology, Cambridge, MA, USA.
Anastasiya BelyaevaMassachusetts Institute of Technology, Cambridge, MA, USA.
Saradha VenkatachalapathyMechanobiology Institute, National University of Singapore, Singapore, Singapore.
Karthik DamodaranMechanobiology Institute, National University of Singapore, Singapore, Singapore.
Abigail KatcoffMassachusetts Institute of Technology, Cambridge, MA, USA.
Adityanarayanan RadhakrishnanMassachusetts Institute of Technology, Cambridge, MA, USA.
G V ShivashankarMechanobiology Institute, National University of Singapore, Singapore, Singapore.
Caroline UhlerMassachusetts Institute of Technology, Cambridge, MA, USA. cuhler@mit.edu.ORCID 0000-0002-7008-0216

Funding

Graduate Training in Computational and Systems BiologyT32GM087237 · NIGMS · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI BURGE, CHRISTOPHER B · 2009 to 2023
$4.6M
NIGMS NIH HHS T32 GM087237
6 · The paper itself

Abstract

The development of single-cell methods for capturing different data modalities including imaging and sequencing has revolutionized our ability to identify heterogeneous cell states. Different data modalities provide different perspectives on a population of cells, and their integration is critical for studying cellular heterogeneity and its function. While various methods have been proposed to integrate different sequencing data modalities, coupling imaging and sequencing has been an open challenge. We here present an approach for integrating vastly different modalities by learning a probabilistic coupling between the different data modalities using autoencoders to map to a shared latent space. We validate this approach by integrating single-cell RNA-seq and chromatin images to identify distinct subpopulations of human naive CD4+ T-cells that are poised for activation. Collectively, our approach provides a framework to integrate and translate between data modalities that cannot yet be measured within the same cell for diverse applications in biomedical discovery.

Indexed as

AlgorithmsSingle-Cell AnalysisCD4-Positive T-LymphocytesCell NucleusChromatinGene Expression ProfilingGene Expression RegulationHumansPrincipal Component AnalysisReproducibility of ResultsROC CurveSequence Analysis, RNAChromatin

Identifiers

PMID33397893
PMCPMC7782789

What OpenQuestion holds

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LicenceCC BY
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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.