Evidence map›Paper›PMID 36991084›Full record

ArticleScientific reports2023

Automated high-throughput image processing as part of the screening platform for personalized oncology.

Marcel P Schilling, Razan El Khaled El Faraj, Joaquín Eduardo Urrutia Gómez, Steffen J Sonnentag, Fei Wang, Britta Nestler, Véronique Orian-Rousseau, Anna A Popova, Pavel A Levkin, Markus Reischl

Abstract read
In one paragraph

Article in Scientific reports, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Review
  2. Article
  3. 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

10 authors.

Marcel P SchillingInstitute for Automation and Applied Informatics, Karlsruhe Institute of Technology, 76344, Eggenstein-Leopoldshafen, Germany. marcel.schilling@kit.edu.
Razan El Khaled El FarajInstitute of Biological and Chemical Systems - Functional Molecular Systems, Karlsruhe Institute of Technology, 76344, Eggenstein-Leopoldshafen, Germany.
Joaquín Eduardo Urrutia GómezInstitute of Biological and Chemical Systems - Functional Molecular Systems, Karlsruhe Institute of Technology, 76344, Eggenstein-Leopoldshafen, Germany.
Steffen J SonnentagInstitute of Biological and Chemical Systems - Functional Molecular Systems, Karlsruhe Institute of Technology, 76344, Eggenstein-Leopoldshafen, Germany.
Fei WangInstitute for Applied Materials, Karlsruhe Institute of Technology, 76131, Karlsruhe, Germany.
Britta NestlerInstitute for Applied Materials, Karlsruhe Institute of Technology, 76131, Karlsruhe, Germany.
Véronique Orian-RousseauInstitute of Biological and Chemical Systems - Functional Molecular Systems, Karlsruhe Institute of Technology, 76344, Eggenstein-Leopoldshafen, Germany.
Anna A PopovaInstitute of Biological and Chemical Systems - Functional Molecular Systems, Karlsruhe Institute of Technology, 76344, Eggenstein-Leopoldshafen, Germany.
Pavel A LevkinInstitute of Biological and Chemical Systems - Functional Molecular Systems, Karlsruhe Institute of Technology, 76344, Eggenstein-Leopoldshafen, Germany.
Markus ReischlInstitute for Automation and Applied Informatics, Karlsruhe Institute of Technology, 76344, Eggenstein-Leopoldshafen, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cancer is a devastating disease and the second leading cause of death worldwide. However, the development of resistance to current therapies is making cancer treatment more difficult. Combining the multi-omics data of individual tumors with information on their in-vitro Drug Sensitivity and Resistance Test (DSRT) can help to determine the appropriate therapy for each patient. Miniaturized high-throughput technologies, such as the droplet microarray, enable personalized oncology. We are developing a platform that incorporates DSRT profiling workflows from minute amounts of cellular material and reagents. Experimental results often rely on image-based readout techniques, where images are often constructed in grid-like structures with heterogeneous image processing targets. However, manual image analysis is time-consuming, not reproducible, and impossible for high-throughput experiments due to the amount of data generated. Therefore, automated image processing solutions are an essential component of a screening platform for personalized oncology. We present our comprehensive concept that considers assisted image annotation, algorithms for image processing of grid-like high-throughput experiments, and enhanced learning processes. In addition, the concept includes the deployment of processing pipelines. Details of the computation and implementation are presented. In particular, we outline solutions for linking automated image processing for personalized oncology with high-performance computing. Finally, we demonstrate the advantages of our proposal, using image data from heterogeneous practical experiments and challenges.

Indexed as

AlgorithmsNeoplasmsComputer SystemsHumansImage Processing, Computer-AssistedLearning

Identifiers

PMID36991084
PMCPMC10060403

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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.