Evidence map›Paper›PMID 30418432›Full record

ArticleNature biotechnology2018

ClampFISH detects individual nucleic acid molecules using click chemistry-based amplification.

Sara H Rouhanifard, Ian A Mellis, Margaret Dunagin, Sareh Bayatpour, Connie L Jiang, Ian Dardani, Orsolya Symmons, Benjamin Emert, Eduardo Torre, Allison Cote and 3 more

Open access · greenAbstract read
In one paragraph

Article in Nature biotechnology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed
6.4field-weighted citation impact, top 2% 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

50 citing papers in PubMed, 148 citations in OpenAlex.

  1. Immunophenotyping by Spatial Biology.Methods in molecular biology (Clifton, N.J.) · 2027
    Article
  2. Review
  3. Review
  4. Review
  5. Applications and development of in situ nucleic acid visualization techniques.Frontiers in bioengineering and biotechnology · 2026
    Review
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. Review
  15. Article
  16. Image-based 3D genomics through chromatin tracing.Nature reviews. Methods primers · 2024
    Article
  17. Article
  18. Review
  19. The dawn of spatial omics.Science (New York, N.Y.) · 2023
    Review
  20. Recent Advances in High-sensitivityActa histochemica et cytochemica · 2023
    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

13 authors at 2 institutions in 1 country.

Sara H RouhanifardDepartment of Bioengineering, University of Pennsylvania, Philadelphia Pennsylvania, USA.ORCID http://orcid.org/0000-0002-6991-4877
Ian A MellisDepartment of Bioengineering, University of Pennsylvania, Philadelphia Pennsylvania, USA.ORCID http://orcid.org/0000-0002-6239-4821
Margaret DunaginDepartment of Bioengineering, University of Pennsylvania, Philadelphia Pennsylvania, USA.
Sareh BayatpourDepartment of Bioengineering, University of Pennsylvania, Philadelphia Pennsylvania, USA.
Connie L JiangDepartment of Bioengineering, University of Pennsylvania, Philadelphia Pennsylvania, USA.
Ian DardaniDepartment of Bioengineering, University of Pennsylvania, Philadelphia Pennsylvania, USA.
Orsolya SymmonsDepartment of Bioengineering, University of Pennsylvania, Philadelphia Pennsylvania, USA.
Benjamin EmertDepartment of Bioengineering, University of Pennsylvania, Philadelphia Pennsylvania, USA.
Eduardo TorreDepartment of Bioengineering, University of Pennsylvania, Philadelphia Pennsylvania, USA.
Allison CoteDepartment of Bioengineering, University of Pennsylvania, Philadelphia Pennsylvania, USA.
Alessandra SullivanAltius Institute for Biomedical Sciences, Seattle, Washington, USA.
John A StamatoyannopoulosAltius Institute for Biomedical Sciences, Seattle, Washington, USA.
Arjun RajDepartment of Bioengineering, University of Pennsylvania, Philadelphia Pennsylvania, USA.ORCID http://orcid.org/0000-0002-2915-6960
University of Pennsylvania · USAltius Institute for Biomedical Sciences · US

Funding

Project-002RM1HG007743 · NHGRI · UNIVERSITY OF WASHINGTON · PI STAMATOYANNOPOULOS, JOHN A · 2015 to 2019
$10.1M
Training Program in Computational GenomicsT32HG000046 · NHGRI · UNIVERSITY OF PENNSYLVANIA · PI JUNHYONG KIM, Mingyao Li · 1999 to 2026
$9.5M
HEMATOPOIESIS TRAINING GRANTT32DK007780 · NIDDK · UNIVERSITY OF PENNSYLVANIA · PI TONG, WEI · 1999 to 2023
$6.7M
High-content optical pooled genome-wide screens of SARS-CoV-2 infectionR01HG009283 · NHGRI · BROAD INSTITUTE, INC. · PI BLAINEY, PAUL CLARK · 2017 to 2020
$4.8M
Engineering and visualizing genome folding at high spatiotemporal resolutionU01HL129998 · NHLBI · UNIVERSITY OF PENNSYLVANIA · PI BLOBEL, GERD A, PHILLIPS-CREMINS, JENNIFER ELIZABETH · 2015 to 2019
$4.2M
Validation and development of single nucleotide variant RNA FISH in single cells in culture and tissueR33EB019767 · NIBIB · UNIVERSITY OF PENNSYLVANIA · PI RAJ, ARJUN · 2014 to 2016
$1.1M
Uncovering the localization and mechanism of RNA editingF32GM120929 · NIGMS · UNIVERSITY OF PENNSYLVANIA · PI ROUHANIFARD, SARA HAKIM · 2017 to 2018
$110k
Single-molecule resolution of RNA editing of mRNAs: visualizing GRIA2 editing in situ in ALSF30NS100595 · NINDS · UNIVERSITY OF PENNSYLVANIA · PI MELLIS, IAN ALEXANDER · 2017 to 2019
$108k
NHGRI NIH HHS R01 HG009283NHGRI NIH HHS RM1 HG007743NHGRI NIH HHS T32 HG000046NHLBI NIH HHS U01 HL129998NIBIB NIH HHS R33 EB019767NIDDK NIH HHS T32 DK007780NIGMS NIH HHS F32 GM120929NINDS NIH HHS F30 NS100595
6 · The paper itself

Abstract

Methods for detecting single nucleic acids in cell and tissues, such as fluorescence in situ hybridization (FISH), are limited by relatively low signal intensity and nonspecific probe binding. Here we present click-amplifying FISH (clampFISH), a method for fluorescence detection of nucleic acids that achieves high specificity and high-gain (>400-fold) signal amplification. ClampFISH probes form a 'C' configuration upon hybridization to the sequence of interest in a double helical manner. The ends of the probes are ligated together using bio-orthogonal click chemistry, effectively locking the probes around the target. Iterative rounds of hybridization and click amplify the fluorescence intensity. We show that clampFISH enables the detection of RNA species with low-magnification microscopy and in RNA-based flow cytometry. Additionally, we show that the modular design of clampFISH probes allows multiplexing of RNA and DNA detection, that the locking mechanism prevents probe detachment in expansion microscopy, and that clampFISH can be applied in tissue samples.

Identifiers

PMID30418432
PMCPMC6511493
OpenAlexW2900659847

What OpenQuestion holds

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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.