Evidence map›Paper›PMID 33113917›Full record

ArticleMolecules (Basel, Switzerland)2020

Highly Multiplexed Single-Cell In Situ RNA and DNA Analysis by Consecutive Hybridization.

Lu Xiao, Renjie Liao, Jia Guo

Open access · goldAbstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
0.6field-weighted citation impact, top 34% 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

12 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Multiplexed Single-CellFrontiers in molecular biosciences · 2021
    Review
  12. FISH Going Meso-Scale: A Microscopic Search for Chromatin Domains.Frontiers in cell and developmental biology · 2021
    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

3 authors at 1 institution in 1 country.

Lu XiaoBiodesign Institute & School of Molecular Sciences, Arizona State University, Tempe, AZ 85287, USA.
Renjie LiaoBiodesign Institute & School of Molecular Sciences, Arizona State University, Tempe, AZ 85287, USA.
Jia GuoBiodesign Institute & School of Molecular Sciences, Arizona State University, Tempe, AZ 85287, USA.ORCID 0000-0001-8036-5349
Arizona State University · US

Funding

Novel in situ proteomics methods to classify cell types in Alzheimer’s brains - Administrative SupplementR01GM127633 · NIGMS · ARIZONA STATE UNIVERSITY-TEMPE CAMPUS · PI GUO, JIA · 2018 to 2022
$1.8M
NIGMS NIH HHS 1R01GM127633
6 · The paper itself

Abstract

The ability to comprehensively profile nucleic acids in individual cells in their natural spatial contexts is essential to advance our understanding of biology and medicine. Here, we report a novel method for spatial transcriptomics and genomics analysis. In this method, every nucleic acid molecule is detected as a fluorescent spot at its natural cellular location throughout the cycles of consecutive fluorescence in situ hybridization (C-FISH). In each C-FISH cycle, fluorescent oligonucleotide probes hybridize to the probes applied in the previous cycle, and also introduce the binding sites for the next cycle probes. With reiterative cycles of hybridization, imaging and photobleaching, the identities of the varied nucleic acids are determined by their unique color sequences. To demonstrate the feasibility of this method, we show that transcripts or genomic loci in single cells can be unambiguously quantified with 2 fluorophores and 16 C-FISH cycles or with 3 fluorophores and 9 C-FISH cycles. Without any error correction, the error rates obtained using the raw data are close to zero. These results indicate that C-FISH potentially enables tens of thousands (2

Indexed as

Nucleic Acid HybridizationDNAHeLa CellsHumansIn Situ Hybridization, FluorescenceRNASingle-Cell AnalysisDNARNAFISHfluorescence in situ hybridizationgenomic locigenomicstranscriptomicstranscripts

Identifiers

PMID33113917
PMCPMC7660199
OpenAlexW3093476567

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.