Evidence map›Paper›PMID 39027045›Full record

ArticleJournal of pathology informatics2024

A novel Slide-seq based image processing software to identify gene expression at the single cell level.

Th I Götz, X Cong, S Rauber, M Angeli, E W Lang, A Ramming, C Schmidkonz

Abstract read
In one paragraph

Article in Journal of pathology informatics, 2024. 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

7 authors.

Th I GötzDepartment of Internal Medicine, University Hospital Erlangen, Erlangen, Germany.
X CongDepartment of Internal Medicine, University Hospital Erlangen, Erlangen, Germany.
S RauberDepartment of Internal Medicine, University Hospital Erlangen, Erlangen, Germany.
M AngeliDepartment of Internal Medicine, University Hospital Erlangen, Erlangen, Germany.
E W LangCIML Group, Biophysics, University of Regensburg, 93040 Regensburg, Germany.
A RammingDepartment of Internal Medicine, University Hospital Erlangen, Erlangen, Germany.
C SchmidkonzDepartment of Nuclear Medicine, University Hospital Erlangen, 91054 Erlangen, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Analysis of gene expression at the single-cell level could help predict the effectiveness of therapies in the field of chronic inflammatory diseases such as arthritis. Here, we demonstrate an adopted approach for processing images from the Slide-seq method. Using a puck, which consists of about 50,000 DNA barcode beads, an RNA sequence of a cell is to be read. The pucks are repeatedly brought into contact with liquids and then recorded with a conventional epifluorescence microscope. The image analysis initially consists of stitching the partial images of a sequence recording, registering images from different sequences, and finally reading out the bases. The new method enables the use of an inexpensive epifluorescence microscope instead of a confocal microscope.

Indexed as

Cell segmentationDeep neural networksDNN complexityPruningSlide-seq

Identifiers

PMID39027045
PMCPMC11254742

What OpenQuestion holds

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Registered trials

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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.