Evidence map›Paper›PMID 42625371›Full record

ArticleBioinformatics (Oxford, England)2026

SeqUIaSCOPE: multi-omics data integration platform for single-patient clinical oncology pathway exploration.

Kateřina Jurásková, Petra Pokorná, Kristián Kováč, Nicolas Blavet, Anna Molíková, Martin Demko, Vojtěch Bystrý

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 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

7 authors.

Kateřina JuráskováCentral European Institute of Technology, Masaryk University, Brno 625 00, Czech Republic.ORCID 0009-0000-8250-1076
Petra PokornáCentral European Institute of Technology, Masaryk University, Brno 625 00, Czech Republic.
Kristián KováčInstitute of Computer Science, Masaryk University, Brno 628 00, Czech Republic.
Nicolas BlavetCentral European Institute of Technology, Masaryk University, Brno 625 00, Czech Republic.ORCID 0000-0003-2199-9119
Anna MolíkováCentral European Institute of Technology, Masaryk University, Brno 625 00, Czech Republic.
Martin DemkoCentral European Institute of Technology, Masaryk University, Brno 625 00, Czech Republic.
Vojtěch BystrýCentral European Institute of Technology, Masaryk University, Brno 625 00, Czech Republic.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

summarySeqUIaSCOPE is an open-source platform designed for routine clinical oncology diagnostics through case-centric integration and visualization of genomic variants, fusion events, and expression profiles. The platform combines molecular-level validation via embedded genome browsing with systems-level interpretation through dynamic pathway visualization, enabling geneticists to assess how alterations converge across biological networks. Flexible reporting with customizable templates accommodates diverse institutional requirements, while secure cluster-based or local deployment ensures compliance with data protection policies, making advanced multi-omics diagnostics accessible to academic and clinical institutions. AVAILABILITY AND IMPLEMENTATION: SeqUIaSCOPE is freely available on GitHub at https://github.com/BioIT-CEITEC/sequiascope under the MIT license and archived at Zenodo (https://zenodo.org/records/21338445). Due to the sensitive nature of patient data, the repository provides simulated datasets that mimic the structure of real clinical data for testing and exploration. Documentation and a live demo accompany these datasets, allowing users to explore the application without any prior setup. The repository also includes a Helm chart for Kubernetes deployment and Docker containers for local deployment, ensuring compatibility across Linux, macOS, and Windows. No user registration is required, and all data remains on local or institutional infrastructure.

Indexed as

Computational BiologyGenomicsMedical OncologyNeoplasmsSoftwareHumansMultiomics

Identifiers

PMID42625371
PMCPMC13537515

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.