Evidence map›Paper›PMID 42681455›Full record

ArticleMethods in molecular biology (Clifton, N.J.)2026

Use of Automated BaseScope Assay on the Leica BOND RX.

Elizabeth J Soilleux, Julia Jones

Abstract read
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In one paragraph

Article in Methods in molecular biology (Clifton, N.J.), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

2 authors.

Elizabeth J SoilleuxDepartment of Pathology, University of Cambridge, Cambridge, CB2 0SP, UK. ejs17@cam.ac.uk.
Julia JonesCancer Research UK Cambridge Institute, University of Cambridge, Robinson Way, Cambridge, CB2 0RE, UK.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The in situ hybridization assay, BaseScope™, detects RNA transcripts in their spatial context, in settings in which enhanced detection is required. Such high sensitivity might be necessary because the target has: (a) low copy number of the target nucleic acid sequence in the cells of interest makes detection challenging with other methodologies, (b) a short target nucleic acid sequence (e.g., 50-300 nucleotides) limiting the number of probes that can be placed along it, (c) very closely related sequences from which it needs to be specifically discriminated. BaseScope™ enables the targeting of RNA sequences using as few as one to three pairs of 18-25 bp antisense oligonucleotide probes, combined with a highly sensitive chromogenic detection method. This assay can be performed on either the Leica BOND RX or the Ventana Discovery Ultra staining platforms; however, this chapter specifically focuses on the automated BaseScope™ assay using the Leica BOND RX platform.

Indexed as

In Situ HybridizationRNAAutomationHumansRNABaseScope™FusionHigh sensitivityMutationPolymorphismTranscript

Identifiers

PMID42681455

What OpenQuestion holds

Textmetadata
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.