48: Mainstreaming Clinical Genetic Testing: A Framework for Care
Base by Base16 Juni 2025

48: Mainstreaming Clinical Genetic Testing: A Framework for Care

Mackley MP et al., Genetics in Medicine - A consensus-driven conceptual framework from Canadian genetics experts describing four models for mainstreaming clinical genetic testing and the variables that determine which model fits specific clinical scenarios. Key terms: mainstreaming, genetic testing, clinical genetics, service delivery, framework.

Study Highlights:
An expert focus group and consensus process were used to develop a unified framework for mainstreaming clinical genetic testing. Thirty-five individuals representing 20 clinical genetics services contributed to delineating diagnostic care pathway stages and influencing variables. The framework defines four generalizable mainstreaming models with increasing involvement of nongeneticist clinicians. Variables across patient, disease, test, report, clinician, and system domains inform model suitability and transitions over time.

Conclusion:
The framework offers a standardized taxonomy to guide design, implementation, and evaluation of mainstreaming programs so genetics resources can be optimally utilized and patient access and care improved; real-world evaluation and broader stakeholder engagement are needed.

Music:
Enjoy the music based on this article at the end of the episode.

Article title:
Mainstreaming of clinical genetic testing: A conceptual framework

First author:
Mackley MP

Journal:
Genetics in Medicine

DOI:
10.1016/j.gim.2025.101465

Reference:
Mackley MP, Richer J, Guerin A, et al. Mainstreaming of clinical genetic testing: A conceptual framework. Genetics in Medicine. 2025. DOI: https://doi.org/10.1016/j.gim.2025.101465

License:
This episode is based on an open-access article published under the Creative Commons Attribution 4.0 International License (CC BY 4.0) – https://creativecommons.org/licenses/by/4.0/

Support:
Base by Base – Stripe donations: https://donate.stripe.com/7sY4gz71B2sN3RWac5gEg00

Official website https://basebybase.com

On PaperCast Base by Base you'll discover the latest in genomics, functional genomics, structural genomics, and proteomics.

Episode link: https://basebybase.com/episodes/mainstreaming-clinical-genetic-testing-framework

QC:
This episode was checked against the original article PDF and publication metadata for the episode release published on 2025-06-16.

QC Scope:
- article metadata and core scientific claims from the narration
- excludes analogies, intro/outro, and music
- transcript coverage: Audited the transcript sections that describe the mainstreaming framework, the four models (to-test, to-result, to-navigation, autonomous), the diagnostic care pathway stages, the influencing variables, practical examples (cancer/autism), safety nets (VUS), and lab report redesign plus limitations.
- transcript topics: Definition and rationale for mainstreaming in clinical genetics; Four-stage diagnostic care pathway: assessment, pretesting, laboratory, post-testing; Four mainstreaming models: to-test, to-result, to-navigation, autonomous; Variables influencing model suitability (patient, disease, test, report, clinician, system); Examples and scenario mapping (cancer, autism spectrum disorder); Safety nets and lab report design to aid non-geneticists

QC Summary:
- factual score: 10/10
- metadata score: 10/10
- supported core claims: 6
- claims flagged for review: 0
- metadata checks passed: 4
- metadata issues found: 0

Metadata Audited:
- article_doi
- article_title
- article_journal
- license

Factual Items Audited:
- Four generalizable mainstreaming models with progressive involvement of genetics services
- Four-stage diagnostic care pathway: assessment, pretesting, laboratory, post-testing
- Six influencing variables (patient, disease, test, diagnostic test...

Det här avsnittet är hämtat från ett öppet RSS-flöde och publiceras inte av Podme. Det kan innehålla reklam.

Avsnitt(462)

461: Adult Ank3 loss quiets neurons and lowers a myelin protein

461: Adult Ank3 loss quiets neurons and lowers a myelin protein

Yoon et al., Proceedings of the National Academy of Sciences - ANK3, which encodes the scaffolding protein ankyrin-G, is a major risk gene for bipolar disorder and schizophrenia, yet what it does in a...

24 Sep 24min

460: The lupus variant that also sharpens antiviral defense

460: The lupus variant that also sharpens antiviral defense

Virolainen et al., The American Journal of Human Genetics - A lupus signal on chromosome 11p15 narrows to a coding haplotype in IRF7 that most people in the world carry. This study shows the risk form...

21 Sep 24min

459: Cerebral palsy genetics: 515 candidate genes, evidence for 89

459: Cerebral palsy genetics: 515 candidate genes, evidence for 89

Arterbery et al., The American Journal of Human Genetics - Hundreds of genes have been reported as causes of cerebral palsy, yet there is no agreed model of what a pathogenic variant in a child with C...

13 Sep 24min

458: Somatic or inherited? Reading TP53 risk from shared DNA

458: Somatic or inherited? Reading TP53 risk from shared DNA

MacGregor et al., The American Journal of Human Genetics - Pathogenic TP53 variants found in blood have long been read as inherited Li-Fraumeni alleles, but many turn out to be somatic clones that gre...

10 Sep 25min

457: A deletion that raises Alzheimer risk, a duplication that lowers it

457: A deletion that raises Alzheimer risk, a duplication that lowers it

Quenez O et al., The American Journal of Human Genetics - Rare copy-number variants were called from 22,319 exomes covering early-onset Alzheimer disease, late-onset disease and unaffected controls, t...

9 Sep 24min

456: Beyond exons: where heritability hides as traits get more polygenic

456: Beyond exons: where heritability hides as traits get more polygenic

Fuhrer J et al., The American Journal of Human Genetics - Across 34 complex traits and disorders, a MiXeR-based framework partitions SNP heritability over 74 functional annotations and finds that exon...

8 Sep 45min

455: Agentic genomics: the bottleneck moves from code to judgment

455: Agentic genomics: the bottleneck moves from code to judgment

Corpas M et al., Cell Genomics - A Perspective arguing that autonomous AI agents which discover, configure and chain bioinformatics operations from natural-language instructions have shifted the bottl...

7 Sep 13min

454: Efavirenz retarda a doença priônica mexendo no colesterol do cérebro [PT]

454: Efavirenz retarda a doença priônica mexendo no colesterol do cérebro [PT]

Ali T et al., JCI Insight - Um antirretroviral aprovado para HIV, dado por via oral em microdose, prolongou a sobrevida de camundongos que carregam a proteína priônica humana e foram infectados com pr...

2 Sep 17min

Populärt inom Vetenskap

dumma-manniskor
p3-dystopia
rss-mottagningen
allt-du-velat-veta
angestpodden
rss-ronden
kapitalet-en-podd-om-ekonomi
det-morka-psyket
rss-ufobortom-rimligt-tvivel
svd-nyhetsartiklar
4health-med-anna-sparre
bildningspodden
rss-vetenskapsradion
rss-geopodden-2
sexet
rss-vetenskapsradion-2
rss-odla
ufo-sverige
rss-spraket
ideer-som-forandrar-varlden