Evidence map›Paper›PMID 36216958›Full record

ArticleNature methods2022

Light-Seq: light-directed in situ barcoding of biomolecules in fixed cells and tissues for spatially indexed sequencing.

Jocelyn Y Kishi, Ninning Liu, Emma R West, Kuanwei Sheng, Jack J Jordanides, Matthew Serrata, Constance L Cepko, Sinem K Saka, Peng Yin

Open access · hybridAbstract read
In one paragraph

Article in Nature methods, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed
5.4field-weighted citation impact, top 3% 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

47 citing papers in PubMed, 65 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Review
  5. Review
  6. dbverse scales spatial omics analysis with embedded analytical databases.bioRxiv : the preprint server for biology · 2026
    Article
  7. Review
  8. Review
  9. Spatially tunable multiomic sequencing using light-driven combinatorial barcoding of molecules in tissues.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  10. Review
  11. A Guide for Spatial Omics Technologies: Innovation, Evaluation, and Application.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Review
  12. Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Review
  19. Review
  20. 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

9 authors at 4 institutions in 3 countries.

Jocelyn Y Kishi *Wyss Institute for Biologically Inspired Engineering, Harvard University, Boston, MA, USA. jocelyn.y.kishi@gmail.com.ORCID 0000-0003-4352-1159
Ninning Liu *Wyss Institute for Biologically Inspired Engineering, Harvard University, Boston, MA, USA.
Emma R West *Department of Genetics, Blavatnik Institute, Harvard Medical School, Boston, MA, USA.
Kuanwei ShengWyss Institute for Biologically Inspired Engineering, Harvard University, Boston, MA, USA.ORCID 0000-0002-7155-9915
Jack J JordanidesWyss Institute for Biologically Inspired Engineering, Harvard University, Boston, MA, USA.
Matthew SerrataWyss Institute for Biologically Inspired Engineering, Harvard University, Boston, MA, USA.
Constance L CepkoDepartment of Genetics, Blavatnik Institute, Harvard Medical School, Boston, MA, USA. cepko@genetics.med.harvard.edu.ORCID 0000-0002-9945-6387
Sinem K SakaWyss Institute for Biologically Inspired Engineering, Harvard University, Boston, MA, USA. sinem.saka@embl.de.ORCID 0000-0002-5017-379X
Peng YinWyss Institute for Biologically Inspired Engineering, Harvard University, Boston, MA, USA. py@hms.harvard.edu.ORCID 0000-0002-2769-6357
Howard Hughes Medical Institute · USEuropean Bioinformatics Institute · GBHarvard University · USInspire Institute · US

Funding

High-throughput single-molecule protein identification via super-resolution imagingDP1GM133052 · NIGMS · HARVARD UNIVERSITY · PI YIN, PENG · 2018 to 2022
$6.6M
Platform technologies for scalable highly multiplexed proteomic phenotyping of the brainRF1MH128861 · NIMH · HARVARD UNIVERSITY · PI CHUNG, KWANGHUN, DONG, HONG-WEI · 2021 to 2021
$5.5M
Multiplexed Nanoscale Protein Mapping Through Expansion Microscopy and Immuno-SABERRF1MH124606 · NIMH · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI BOYDEN, EDWARD S., YIN, PENG · 2020 to 2020
$2.7M
Decoding chromosome structure with multiplexed super-resolution microscopyR01GM124401 · NIGMS · HARVARD UNIVERSITY · PI YIN, PENG · 2018 to 2021
$2.5M
High-Throughput, Highly Multiplexed In Situ Proteomic Imaging of Human TissuesUH3CA255133 · NCI · HARVARD UNIVERSITY · PI YIN, PENG · 2020 to 2021
$1.1M
High-Throughput, Highly Multiplexed In Situ Proteomic Imaging of Human TissuesUG3HL145600 · NHLBI · HARVARD UNIVERSITY · PI YIN, PENG · 2018 to 2019
$833k
Howard Hughes Medical InstituteNCI NIH HHS UH3 CA255133NHLBI NIH HHS UG3 HL145600NIGMS NIH HHS DP1 GM133052NIGMS NIH HHS R01 GM124401NIMH NIH HHS RF1 MH124606NIMH NIH HHS RF1 MH128861
6 · The paper itself

Abstract

We present Light-Seq, an approach for multiplexed spatial indexing of intact biological samples using light-directed DNA barcoding in fixed cells and tissues followed by ex situ sequencing. Light-Seq combines spatially targeted, rapid photocrosslinking of DNA barcodes onto complementary DNAs in situ with a one-step DNA stitching reaction to create pooled, spatially indexed sequencing libraries. This light-directed barcoding enables in situ selection of multiple cell populations in intact fixed tissue samples for full-transcriptome sequencing based on location, morphology or protein stains, without cellular dissociation. Applying Light-Seq to mouse retinal sections, we recovered thousands of differentially enriched transcripts from three cellular layers and discovered biomarkers for a very rare neuronal subtype, dopaminergic amacrine cells, from only four to eight individual cells per section. Light-Seq provides an accessible workflow to combine in situ imaging and protein staining with next generation sequencing of the same cells, leaving the sample intact for further analysis post-sequencing.

Indexed as

DNAHigh-Throughput Nucleotide SequencingAnimalsDNA, ComplementaryMiceDNADNA, Complementary

Identifiers

PMID36216958
PMCPMC9636025
OpenAlexW4304084269

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.