Evidence map›Paper›PMID 31263868›Full record

ReviewBriefings in bioinformatics2020

Implementing the FAIR Data Principles in precision oncology: review of supporting initiatives.

Charles Vesteghem, Rasmus Froberg Brøndum, Mads Sønderkær, Mia Sommer, Alexander Schmitz, Julie Støve Bødker, Karen Dybkær, Tarec Christoffer El-Galaly, Martin Bøgsted

Abstract readReview
In one paragraph

Review in Briefings in bioinformatics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed, 1 pooled it
–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

36 citing papers in PubMed, 1 synthesis or guideline pooled it.

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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

9 authors.

Charles VesteghemDepartment of Clinical Medicine, Aalborg University, Denmark.
Rasmus Froberg BrøndumDepartment of Haematology, Aalborg University Hospital, Denmark.
Mads SønderkærDepartment of Haematology, Aalborg University Hospital, Denmark.
Mia SommerDepartment of Clinical Medicine, Aalborg University, Denmark.
Alexander SchmitzDepartment of Haematology, Aalborg University Hospital, Denmark.
Julie Støve BødkerDepartment of Haematology, Aalborg University Hospital, Denmark.
Karen DybkærDepartment of Clinical Medicine, Aalborg University, Denmark.
Tarec Christoffer El-GalalyDepartment of Clinical Medicine, Aalborg University, Denmark.
Martin BøgstedDepartment of Clinical Medicine, Aalborg University, Denmark.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Compelling research has recently shown that cancer is so heterogeneous that single research centres cannot produce enough data to fit prognostic and predictive models of sufficient accuracy. Data sharing in precision oncology is therefore of utmost importance. The Findable, Accessible, Interoperable and Reusable (FAIR) Data Principles have been developed to define good practices in data sharing. Motivated by the ambition of applying the FAIR Data Principles to our own clinical precision oncology implementations and research, we have performed a systematic literature review of potentially relevant initiatives. For clinical data, we suggest using the Genomic Data Commons model as a reference as it provides a field-tested and well-documented solution. Regarding classification of diagnosis, morphology and topography and drugs, we chose to follow the World Health Organization standards, i.e. ICD10, ICD-O-3 and Anatomical Therapeutic Chemical classifications, respectively. For the bioinformatics pipeline, the Genome Analysis ToolKit Best Practices using Docker containers offer a coherent solution and have therefore been selected. Regarding the naming of variants, we follow the Human Genome Variation Society's standard. For the IT infrastructure, we have built a centralized solution to participate in data sharing through federated solutions such as the Beacon Networks.

Indexed as

Precision MedicineComputational BiologyGenome, HumanGenomicsHumansInformation DisseminationMedical OncologyNeoplasmsdata sharingFAIR Data Principlesgenomicsprecision oncologystandards

Identifiers

PMID31263868
PMCPMC7299292

What OpenQuestion holds

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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.