Evidence map›Paper›PMID 38200118›Full record

ArticleNature biotechnology2024

Prediction of single-cell RNA expression profiles in live cells by Raman microscopy with Raman2RNA.

Koseki J Kobayashi-Kirschvink, Charles S Comiter, Shreya Gaddam, Taylor Joren, Emanuelle I Grody, Johain R Ounadjela, Ke Zhang, Baoliang Ge, Jeon Woong Kang, Ramnik J Xavier and 4 more

Open access · greenAbstract read
In one paragraph

Article in Nature biotechnology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 49 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
49citing papers in PubMed, 1 pooled it
45.0field-weighted citation impact, top 1% of its field
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

49 citing papers in PubMed, 1 synthesis or guideline pooled it, 69 citations in OpenAlex.

  1. Pooled it
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  6. PLANCK: super-multiplex optical imaging without labeling.bioRxiv : the preprint server for biology · 2026
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  20. Vibrational Probes in Bioimaging and Chemical Biology.Chemical & biomedical imaging · 2025
    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

14 authors at 2 institutions in 1 country.

Koseki J Kobayashi-KirschvinkKlarman Cell Observatory, Broad Institute of MIT and Harvard, Cambridge, MA, USA. kkobayas@broadinstitute.org.ORCID http://orcid.org/0000-0001-6590-3823
Charles S ComiterKlarman Cell Observatory, Broad Institute of MIT and Harvard, Cambridge, MA, USA.ORCID http://orcid.org/0000-0003-4201-1739
Shreya GaddamKlarman Cell Observatory, Broad Institute of MIT and Harvard, Cambridge, MA, USA.
Taylor JorenKlarman Cell Observatory, Broad Institute of MIT and Harvard, Cambridge, MA, USA.
Emanuelle I GrodyKlarman Cell Observatory, Broad Institute of MIT and Harvard, Cambridge, MA, USA.ORCID http://orcid.org/0000-0002-7177-3268
Johain R OunadjelaKlarman Cell Observatory, Broad Institute of MIT and Harvard, Cambridge, MA, USA.
Ke ZhangKlarman Cell Observatory, Broad Institute of MIT and Harvard, Cambridge, MA, USA.
Baoliang GeDepartment of Mechanical and Biological Engineering, Massachusetts Institute of Technology, Cambridge, MA, USA.
Jeon Woong KangLaser Biomedical Research Center, G. R. Harrison Spectroscopy Laboratory, Massachusetts Institute of Technology, Cambridge, MA, USA.ORCID http://orcid.org/0000-0003-2012-9023
Ramnik J XavierKlarman Cell Observatory, Broad Institute of MIT and Harvard, Cambridge, MA, USA.
Peter T C SoLaser Biomedical Research Center, G. R. Harrison Spectroscopy Laboratory, Massachusetts Institute of Technology, Cambridge, MA, USA.
Tommaso BiancalaniKlarman Cell Observatory, Broad Institute of MIT and Harvard, Cambridge, MA, USA. biancalt@gene.com.ORCID http://orcid.org/0000-0001-9104-9755
Jian ShuKlarman Cell Observatory, Broad Institute of MIT and Harvard, Cambridge, MA, USA. jian.shu@mgh.harvard.edu.ORCID http://orcid.org/0000-0001-9390-9333
Aviv RegevKlarman Cell Observatory, Broad Institute of MIT and Harvard, Cambridge, MA, USA. aviv.regev.sc@gmail.com.ORCID http://orcid.org/0000-0003-3293-3158
Broad Institute · USMassachusetts Institute of Technology · US

Funding

Tool and Technology Development CoreU19MH114821 · NIMH · COLD SPRING HARBOR LABORATORY · PI HUANG, Z JOSH · 2017 to 2021
$64.5M
Pilot & Feasibility ProgramP30DK043351 · NIDDK · MASSACHUSETTS GENERAL HOSPITAL · PI RAYMOND T CHUNG · 1991 to 2026
$35.3M
Wide-Field Short-Wave Infrared (SWIR) multiphoton (MP) tissue imagingP41EB015871 · NIBIB · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI SO, PETER T. · 2012 to 2021
$11.3M
Implementation of Slide-seq for high-resolution, whole-transcriptome human tissue maps.UH3CA246632 · NCI · BROAD INSTITUTE, INC. · PI MACOSKO, EVAN Z · 2019 to 2021
$1.9M
Single-cell label-free identification of senescence by Raman microscopy and spatial genomicsUG3CA275687 · NCI · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI SO, PETER T. · 2022 to 2023
$1.1M
Dissecting and reconstructing the molecular roadmaps of cellular reprogramming to iPSCs in single-cell resolutionR00HD096049 · NICHD · MASSACHUSETTS GENERAL HOSPITAL · PI SHU, JIAN · 2021 to 2023
$721k
NCI NIH HHS UG3 CA275687NCI NIH HHS UH3 CA246632NIBIB NIH HHS P41 EB015871NICHD NIH HHS R00 HD096049NIDDK NIH HHS P30 DK043351NIMH NIH HHS U19 MH114821
6 · The paper itself

Abstract

Single-cell RNA sequencing and other profiling assays have helped interrogate cells at unprecedented resolution and scale, but are inherently destructive. Raman microscopy reports on the vibrational energy levels of proteins and metabolites in a label-free and nondestructive manner at subcellular spatial resolution, but it lacks genetic and molecular interpretability. Here we present Raman2RNA (R2R), a method to infer single-cell expression profiles in live cells through label-free hyperspectral Raman microscopy images and domain translation. We predict single-cell RNA sequencing profiles nondestructively from Raman images using either anchor-based integration with single molecule fluorescence in situ hybridization, or anchor-free generation with adversarial autoencoders. R2R outperformed inference from brightfield images (cosine similarities: R2R >0.85 and brightfield <0.15). In reprogramming of mouse fibroblasts into induced pluripotent stem cells, R2R inferred the expression profiles of various cell states. With live-cell tracking of mouse embryonic stem cell differentiation, R2R traced the early emergence of lineage divergence and differentiation trajectories, overcoming discontinuities in expression space. R2R lays a foundation for future exploration of live genomic dynamics.

Indexed as

Single-Cell AnalysisSpectrum Analysis, RamanAnimalsCell DifferentiationFibroblastsGene Expression ProfilingInduced Pluripotent Stem CellsIn Situ Hybridization, FluorescenceMiceMicroscopyRNASequence Analysis, RNATranscriptomeRNA

Identifiers

PMID38200118
PMCPMC11233426
OpenAlexW4390701876

What OpenQuestion holds

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LicenceTDM
Read underepoch 390

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.