Paper Details

Paper Title

Shariant platform: Enabling evidence sharing across Australian clinical genetic-testing laboratories to support variant interpretation.

Paper Journal Title

Am J Hum Genet

Paper Citation Count

Paper Publication Year

2022

Bio Mention

Mesh Descriptor

Author Name	Affiliation
John Beilby	The University of Western Australia
John Beilby	The University of Western Australia
Tiffany Boughtwood	Australia Murdoch Children's Research Institute
John Christodoulou	University of Sydney, Australia Murdoch Children's Research Institute, University of Melbourne
Mark R Davis	The University of Western Australia
Marcel E Dinger	University of New South Wales
Johanna Hadler
Karin S Kassahn	Australia Adelaide Medical School, The University of Adelaide
Katia Nones	QIMR Berghofer Medical Research Institute
Katia Nones	QIMR Berghofer Medical Research Institute
John V Pearson	QIMR Berghofer Medical Research Institute
John V Pearson	QIMR Berghofer Medical Research Institute
Lesley Rawlings
Zornitza Stark	Australia Victorian Clinical Genetics Services, Murdoch Children's Research Institute, Australia University of Melbourne
Amanda B Spurdle	QIMR Berghofer Medical Research Institute
Amanda B Spurdle	QIMR Berghofer Medical Research Institute

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Dataset	Description	Source Link
ClinVar	ClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publ	Link
ClinVar	ClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.	Link
ClinVar	ClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publ	Link
ClinVar	ClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publ	Link
ClinVar	ClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.	Link
ClinVar	ClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publ	Link
ClinVar	ClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publ	Link
ClinVar	ClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publ	Link
ClinVar	ClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.	Link
ClinVar	ClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publ	Link
ClinVar	ClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.	Link
ClinVar	ClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.	Link
ClinVar	ClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.	Link
ClinVar	ClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.	Link
ClinVar	ClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publ	Link

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