This is a preview of subscription content, access via your institution
Relevant articles
Open Access articles citing this article.
-
The systematic assessment of completeness of public metadata accompanying omics studies in the Gene Expression Omnibus data repository
Genome Biology Open Access 09 September 2025
-
Genomics on FHIR – a feasibility study to support a National Strategy for Genomic Medicine
npj Genomic Medicine Open Access 29 July 2025
-
Towards a standard benchmark for phenotype-driven variant and gene prioritisation algorithms: PhEval - Phenotypic inference Evaluation framework
BMC Bioinformatics Open Access 22 March 2025
Access options
Access Nature and 54 other Nature Portfolio journals
Get Nature+, our best-value online-access subscription
$32.99 / 30 days
cancel any time
Subscribe to this journal
Receive 12 print issues and online access
$259.00 per year
only $21.58 per issue
Buy this article
- Purchase on SpringerLink
- Instant access to full article PDF
Prices may be subject to local taxes which are calculated during checkout

References
Richesson, R. L. et al. J. Am. Med. Inform. Assoc. 20, e226–e231 (2013).
Hripcsak, G. & Albers, D. J. J. Am. Med. Inform. Assoc. 20, 117–121 (2013).
Shivade, C. et al. J. Am. Med. Inform. Assoc. 21, 221–230 (2014).
Wei, W.-Q. & Denny, J. C. Genome Med. 7, 41 (2015).
Richesson, R. L., Sun, J., Pathak, J., Kho, A. N. & Denny, J. C. Artif. Intell. Med. 71, 57–61 (2016).
Rehm, H. L. et al. Cell Genom. 1, 100029 (2021).
Köhler, S. et al. Nucleic Acids Res. 49, D1207–D1217 (2021).
Sioutos, N. et al. J. Biomed. Inform. 40, 30–43 (2007).
Fiume, M. et al. Nat. Biotechnol. 37, 220–224 (2019).
Danecek, P. et al. Bioinformatics 27, 2156–2158 (2011).
Acknowledgements
The authors gratefully acknowledge insight and feedback from Marian H. Adly, Pier Luigi Buttigieg, Janine Lewis, Manuel Posada de la Paz and Maria Taboada. This work was supported by 7RM1HG010860-02 (NHGRI). Additional funding was as follows. P.N.R. was supported by NLM contract 75N97019P00280, NIH NHGRI RM1HG010860, NIH OD R24OD011883 and NIH NICHD 1R01HD103805-01. H.H. was supported by NIH OD R24OD011883. G.I.S. was supported by ELIXIR, the research infrastructure for life-science data. C.G.C. was supported by NIH NCATS U24TR002306. K.C.L. was supported by NIH OD 5UM1OD023221. M.B. was supported by the BioMedIT Network project of the Swiss Institute of Bioinformatics (SIB) and Swiss Personalized Health Network (SPHN). A.H.W. was supported by NIH NHGRI K99HG010157 and NIH NHGRI R00HG010157. C.J.M., M.A.H., M.C.M.-T., J.A.M. and D.D. were supported by NIH NHGRI RM1HG010860 and NIH OD R24OD011883. A.M.-J. was supported by Australian Genomics. Australian Genomics is supported by the National Health and Medical Research Council (GNT1113531). D. Smedley and J.O.B.J. were supported by NIH NHGRI RM1HG010860, NIH OD R24OD011883 and NIH NICHD 1R01HD103805-01. M.D. was supported by NIH NHGRI U54HG004028, NIH NHGRI 5U01HG008473-03 and NIH NCATS OT2TR003434-01S1U54HG008033-01. G.S.B. was supported by the Roy Hill Community Foundation, Angela Wright Bennett Foundation, McCusker Charitable Foundation, Borlaug Foundation and Stan Perron Charitable Foundation. L.B. was supported by NIH NHGRI U41HG006834 (Clinical Genome Resource). M.C. was supported by EMBL-EBI Core Funds and Wellcome Trust GA4GH award number 201535/Z/16/Z. A.H. was supported by NIH NHGRI 1U41HG006627, NIH NHGRI 1U54HG006542 and NIH NHGRI 1RM1HG010860. P.N.S. was supported by The Alan Turing Institute. N.L.H. was supported by NIH NHGRI RM1HG010860, NIH OD R24OD011883 and US Department of Energy Contract DE-AC02-05CH11231. N.P. was supported by Moorfields Eye Charity. N.Q.-R. was supported by EU Horizon 2020 research and innovation programme grant agreement 825575 (EJP-RD). O.E. was supported by NIH grants UL1TR002384, R01CA194547 and P01CA214274, LLS SCOR grants 180078-01 and 7021-20 and Starr Cancer Consortium grant I11-0027. H. Lochmüller was supported by the CIHR Foundation Grant on Precision Health for Neuromuscular Diseases FDN-167281. R.T. was supported by CIHR postdoctoral fellowship award MFE-171275. L.D.S. was supported by Genome Canada and NIH NHGRI U24HG011025. S.O. was supported by AMED. D.P., L.M., A.P., S.B., M.R. and R.K. were supported by EU Horizon 2020 research and innovation programme grant agreements 779257 (Solve-RD) and 825575 (EJP-RD). R.R.F. was supported by NLM contract 75N97019P00280.
Author information
Authors and Affiliations
Consortia
Corresponding authors
Ethics declarations
Competing interests
S.K. is an employee of Ada Health GmbH. N.P. is a director of Phenopolis Ltd. O.E. is supported by Janssen, Johnson & Johnson, Volastra Therapeutics, AstraZeneca and Eli Lilly research grants, and is a scientific advisor and equity holder in Freenome, Owkin, Volastra Therapeutics and One Three Biotech. A.R.M. is an employee of Philips Research North America. O.J.B. is an employee of PhenoTips. M.A. is an editor employed by Wiley. A.S. is an employee of Lifebit Biotech Ltd. The remaining authors declare no competing interests.
Peer review
Peer review information
Nature Biotechnology thanks Kai Wang and the other, anonymous, reviewer(s) for their contribution to the peer review of this work.
Supplementary information
Supplementary Information
Supplementary Tables 1 and 2
Rights and permissions
About this article
Cite this article
Jacobsen, J.O.B., Baudis, M., Baynam, G.S. et al. The GA4GH Phenopacket schema defines a computable representation of clinical data. Nat Biotechnol 40, 817–820 (2022). https://doi.org/10.1038/s41587-022-01357-4
Published:
Issue date:
DOI: https://doi.org/10.1038/s41587-022-01357-4
This article is cited by
-
Towards a standard benchmark for phenotype-driven variant and gene prioritisation algorithms: PhEval - Phenotypic inference Evaluation framework
BMC Bioinformatics (2025)
-
A call to action to scale up research and clinical genomic data sharing
Nature Reviews Genetics (2025)
-
Genomics on FHIR – a feasibility study to support a National Strategy for Genomic Medicine
npj Genomic Medicine (2025)
-
An ontology-based rare disease common data model harmonising international registries, FHIR, and Phenopackets
Scientific Data (2025)
-
The systematic assessment of completeness of public metadata accompanying omics studies in the Gene Expression Omnibus data repository
Genome Biology (2025)