ArticleVirchows Archiv : an international journal of pathology2026
Tissue biobanking: minimum interface requirements for efficient and high-quality support for biomedical research - a white paper.
Article in Virchows Archiv : an international journal of pathology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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.
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.
Who cites it
1 citing paper in PubMed.
- Review
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
15 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Tissue biobanking is essential for biomedical research. Well-defined interfaces and standardised procedures are required to ensure sample quality and the subsequent reproducibility of research results. This paper provides an overview of the key interfaces involved in tissue biobanking workflows, including sample collection, processing, storage, distribution and data management. It outlines the minimum standards required to maintain high-quality samples and associated data, and references relevant national and international guidelines. The paper also addresses the current challenges faced by biobanks, such as harmonisation across institutions, evolving regulatory landscapes, and the integration of digital infrastructure. The primary aim of this work is to present recommendations for the effective implementation and documentation of minimum standards. These recommendations are intended to help biobanks to align with regulatory expectations, optimise operational procedures, and facilitate high-quality, ethically sound biomedical research.
Indexed as
Identifiers
42228140What OpenQuestion holds
Registered trials
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.