Evidence map›Paper›PMID 24578530›Full record

ArticleScience (New York, N.Y.)2014

Highly multiplexed subcellular RNA sequencing in situ.

Je Hyuk Lee, Evan R Daugharthy, Jonathan Scheiman, Reza Kalhor, Joyce L Yang, Thomas C Ferrante, Richard Terry, Sauveur S F Jeanty, Chao Li, Ryoji Amamoto and 9 more

Abstract read
In one paragraph

Article in Science (New York, N.Y.), 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 556 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
556citing papers in PubMed, 1 pooled it
39.4field-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

556 citing papers in PubMed, 1 synthesis or guideline pooled it, 1,005 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Review
  4. Insights Into Spatial Transcriptomics: Exploring Recent Technical Developments and Their Diverse Applications.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2026
    Review
  5. Mapping Embryonic Mouse Lung Development Using Enhanced Spatial Transcriptomics.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Article
  6. Article
  7. Review
  8. Article
  9. Review
  10. Review
  11. Review
  12. Review
  13. Review
  14. Article
  15. Article
  16. Review
  17. Review
  18. Article
  19. 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
  20. Article

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

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

19 authors at 2 institutions in 1 country.

Je Hyuk LeeWyss Institute, Harvard Medical School, Boston, MA 02115, USA.
Evan R Daugharthy
Jonathan Scheiman
Reza Kalhor
Joyce L Yang
Thomas C Ferrante
Richard Terry
Sauveur S F Jeanty
Chao Li
Ryoji Amamoto
Derek T Peters
Brian M Turczyk
Adam H Marblestone
Samuel A Inverso
Amy Bernard
Prashant Mali
Xavier Rios
John Aach
George M Church
Harvard University · USAllen Institute · US

Funding

Medical Scientist Training ProgramT32GM007753 · NIGMS · HARVARD UNIVERSITY (MEDICAL SCHOOL) · PI WALENSKY, LOREN DAVID · 1985 to 2021
$50.0M
Causal Transcriptional Consequences of Human Genetic VariationP50HG005550 · NHGRI · HARVARD MEDICAL SCHOOL · PI CHURCH, GEORGE M · 2010 to 2014
$19.0M
Single-cell sequencing and in situ mapping of RNA transcripts in human brainsU01MH098977 · NIMH · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI ZHANG, KUN · 2012 to 2016
$9.8M
Comparative phenotypic, functional, and molecular analysis of ESC and iPSCRC2HL102815 · NHLBI · BOSTON CHILDREN'S HOSPITAL · PI CHURCH, GEORGE M, COLLINS, JAMES J · 2009 to 2010
$3.4M
Harvard Systems Biology Graduate ProgramT32GM080177 · NIGMS · HARVARD UNIVERSITY · PI MITCHISON, TIMOTHY J, MURRAY, ANDREW W · 2010 to 2019
$2.8M
NHGRI NIH HHS P50 HG005550NHLBI NIH HHS RC2 HL102815NHLBI NIH HHS RC2HL102815NIGMS NIH HHS GM080177NIGMS NIH HHS T32 GM007753NIGMS NIH HHS T32 GM080177NIMH NIH HHS MH098977NIMH NIH HHS U01 MH098977
6 · The paper itself

Abstract

Understanding the spatial organization of gene expression with single-nucleotide resolution requires localizing the sequences of expressed RNA transcripts within a cell in situ. Here, we describe fluorescent in situ RNA sequencing (FISSEQ), in which stably cross-linked complementary DNA (cDNA) amplicons are sequenced within a biological sample. Using 30-base reads from 8102 genes in situ, we examined RNA expression and localization in human primary fibroblasts with a simulated wound-healing assay. FISSEQ is compatible with tissue sections and whole-mount embryos and reduces the limitations of optical resolution and noisy signals on single-molecule detection. Our platform enables massively parallel detection of genetic elements, including gene transcripts and molecular barcodes, and can be used to investigate cellular phenotype, gene regulation, and environment in situ.

Indexed as

TranscriptomeBase SequenceCell LineCells, CulturedDNA, ComplementaryFluorescenceGene Expression ProfilingHumansInduced Pluripotent Stem CellsRNA, MessengerSequence Analysis, RNASingle-Cell AnalysisTranscription Initiation SiteWound HealingDNA, ComplementaryRNA, Messenger

Identifiers

PMID24578530
PMCPMC4140943
OpenAlexW2151013106

What OpenQuestion holds

Textmetadata
LicenceTDM
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.