Evidence map›Paper›PMID 26742656›Full record

ArticleCurrent protocols in cytometry2016

Simultaneous, Single-Cell Measurement of Messenger RNA, Cell Surface Proteins, and Intracellular Proteins.

Kah Teong Soh, Joseph D Tario, Sean Colligan, Orla Maguire, Dalin Pan, Hans Minderman, Paul K Wallace

Abstract read
In one paragraph

Article in Current protocols in cytometry, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
–field-weighted citation impact
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

9 citing papers in PubMed.

  1. Review
  2. Article
  3. Computational strategies for single-cell multi-omics integration.Computational and structural biotechnology journal · 2021
    Review
  4. Article
  5. Article
  6. RNA Flow Cytometry Using the Branched DNA Technique.Methods in molecular biology (Clifton, N.J.) · 2018
    Article
  7. Article
  8. Review
  9. 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

7 authors.

Kah Teong SohDepartment of Flow and Image Cytometry, Roswell Park Cancer Institute, Buffalo, New York.
Joseph D TarioDepartment of Flow and Image Cytometry, Roswell Park Cancer Institute, Buffalo, New York.
Sean ColliganDepartment of Flow and Image Cytometry, Roswell Park Cancer Institute, Buffalo, New York.
Orla MaguireDepartment of Flow and Image Cytometry, Roswell Park Cancer Institute, Buffalo, New York.
Dalin PanDepartment of Flow and Image Cytometry, Roswell Park Cancer Institute, Buffalo, New York.
Hans MindermanDepartment of Flow and Image Cytometry, Roswell Park Cancer Institute, Buffalo, New York.
Paul K WallaceDepartment of Flow and Image Cytometry, Roswell Park Cancer Institute, Buffalo, New York.

Funding

Two-Spirit Films in Indigenous Cancer HealthP30CA016056 · NCI · ROSWELL PARK CANCER INSTITUTE CORP · PI Dean G. Tang · 1985 to 2026
$116.6M
RPCI-UPCI Ovarian Cancer SPOREP50CA159981 · NCI · ROSWELL PARK CANCER INSTITUTE CORP · PI MOYSICH, KIRSTEN B., ODUNSI, KUNLE · 2013 to 2025
$19.6M
NCI NIH HHS 1P50CA159981-01A1NCI NIH HHS 5 P30 CA016056-29NCI NIH HHS P30 CA016056NCI NIH HHS P50 CA159981
6 · The paper itself

Abstract

Nucleic acid content can be quantified by flow cytometry through the use of intercalating compounds; however, measuring the presence of specific sequences has hitherto been difficult to achieve by this methodology. The primary obstacle to detecting discrete nucleic acid sequences by flow cytometry is their low quantity and the presence of high background signals, rendering the detection of hybridized fluorescent probes challenging. Amplification of nucleic acid sequences by molecular techniques such as in situ PCR have been applied to single-cell suspensions, but these approaches have not been easily adapted to conventional flow cytometry. An alternative strategy implements a Branched DNA technique, comprising target-specific probes and sequentially hybridized amplification reagents, resulting in a theoretical 8,000- to 16,000-fold increase in fluorescence signal amplification. The Branched DNA technique allows for the quantification of native and unmanipulated mRNA content with increased signal detection and reduced background. This procedure utilizes gentle fixation steps with low hybridization temperatures, leaving the assayed cells intact to permit their concomitant immunophenotyping. This technology has the potential to advance scientific discovery by correlating potentially small quantities of mRNA with many biological measurements at the single-cell level.

Indexed as

Antigens, CDApoptosisCD8-Positive T-LymphocytesCell CycleCell MembraneComputational BiologyDNAFlow CytometryHumansImmunophenotypingIn Situ HybridizationLeukocytes, MononuclearMembrane ProteinsNucleic Acid HybridizationPhosphorylationPolymerase Chain ReactionAntigens, CDDNAMembrane ProteinsRNA, MessengerBranched DNAflow cytometryin situ hybridizationleukocytesmRNA sequencetarget probetranscription factors

Identifiers

PMID26742656
PMCPMC5556691

What OpenQuestion holds

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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.