Evidence map›Paper›PMID 42094490›Full record

ArticlebioRxiv : the preprint server for biology2026

The GA4GH Categorical Variation Representation Specification: A Unified Computational Framework for Reasoning over Genomic Variant Categories.

Daniel Puthawala, Brendan Reardon, Lawrence Babb, Kori Kuzma, James S Stevenson, Wesley A Goar, Robert H Dolin, Robert R Freimuth, Catherine Procknow, Beth Pitel and 4 more

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 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

14 authors.

Daniel PuthawalaThe Steve and Cindy Rasmussen Institute for Genomic Medicine, Nationwide Children's Hospital, Columbus, OH.ORCID 0000-0002-1823-7124
Brendan ReardonDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA.ORCID 0000-0002-1716-5720
Lawrence BabbMedical and Population Genetics, Broad Institute of MIT and Harvard, Cambridge, MA.ORCID 0000-0002-2455-2227
Kori KuzmaThe Steve and Cindy Rasmussen Institute for Genomic Medicine, Nationwide Children's Hospital, Columbus, OH.ORCID 0000-0002-9954-7449
James S StevensonThe Steve and Cindy Rasmussen Institute for Genomic Medicine, Nationwide Children's Hospital, Columbus, OH.ORCID 0000-0002-2568-6163
Wesley A GoarThe Steve and Cindy Rasmussen Institute for Genomic Medicine, Nationwide Children's Hospital, Columbus, OH.ORCID 0000-0002-9954-3982
Robert H DolinElimu Informatics, El Cerrito, CA.ORCID 0000-0002-6235-6964
Robert R FreimuthMayo Clinic, Rochester, MN.ORCID 0000-0002-9673-5612
Catherine ProcknowEpic Systems,Verona, WI.
Beth PitelMayo Clinic, Rochester, MN.ORCID 0000-0002-5138-824X
Parijat KunduVelsera, Pune, India.ORCID 0000-0003-1944-4579
Akash RampersadOakBioinformatics LLC, Fairfax, VA.ORCID 0009-0001-7554-3419
Eliezer Van AllenDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA.ORCID 0000-0002-0201-4444
Alex H WagnerThe Steve and Cindy Rasmussen Institute for Genomic Medicine, Nationwide Children's Hospital, Columbus, OH.ORCID 0000-0002-2502-8961

Funding

Tracking Ethical Provenance for Sharing Genomic and Health Related DataU24HG011025 · NHGRI · BROAD INSTITUTE, INC. · PI HEIDI L REHM · 2021 to 2026
$8.2M
FHIRCat: Enabling the Semantics of FHIR and Terminologies for Clinical and Translational ResearchR01EB030529 · NIBIB · MAYO CLINIC ROCHESTER · PI FREIMUTH, ROBERT RICHARD · 2021 to 2024
$2.7M
Text Mining and Large Language Models for AI-Driven Evidence-Based Functional Annotation of Clinical VariantsU24CA275783 · NCI · WASHINGTON UNIVERSITY · PI Malachi Griffith, Obi L. Griffith · 2023 to 2026
$2.6M
Development and validation of a computable knowledge framework for genomic medicineR35HG011949 · NHGRI · RESEARCH INST NATIONWIDE CHILDREN'S HOSP · PI WAGNER, ALEX HANDLER · 2021 to 2025
$2.4M
Integrated Knowledge Management Framework for Clinical GenomicsR35HG011899 · NHGRI · MAYO CLINIC ROCHESTER · PI FREIMUTH, ROBERT RICHARD · 2021 to 2025
$2.4M
Accelerating the expert-crowdsourcing of cancer variant interpretation in CIViCU24CA305456 · NCI · WASHINGTON UNIVERSITY · PI Malachi Griffith, Obi L. Griffith · 2025 to 2026
$2.0M
NCI NIH HHS U24 CA275783NCI NIH HHS U24 CA305456NHGRI NIH HHS R35 HG011899NHGRI NIH HHS R35 HG011949NHGRI NIH HHS U24 HG011025NIBIB NIH HHS R01 EB030529Wellcome Trust
6 · The paper itself

Abstract

Categorical variants, or sets of genomic alterations constrained by shared properties, are pervasive across clinical, regulatory, and research domains in the biomedical ecosystem, yet their inconsistent and non-computable representation hinders data interoperability and clinical interpretation. We surveyed genomic knowledgebases spanning regulatory approvals and the biomedical literature and found that categorical variants underpin a substantial proportion of clinical genomics knowledge, but are largely described using incompatible bespoke models. To address this, we developed the GA4GH Categorical Variation Representation Specification (Cat-VRS), a constraint-based framework that provides a unified computable representation for both precise and intentionally broad categories across molecular and systemic variant domains. Cat-VRS enables harmonization of genomic knowledgebases, computable category-based search, and automated matching between assayed variants and categorical entities in clinical and research contexts. By providing a principled, extensible model for categorical variation, Cat-VRS enables computable reasoning over genomic variant categories and establishes a foundation for the standardized representation and exchange of genomic knowledge.

Identifiers

PMID42094490
PMCPMC13142434

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.