Open sharing of clinical genetic data promises to both monitor and eventually improve the reproducibility of variant interpretation among clinical testing laboratories. A significant public data resource has been developed by the NIH ClinVar initiative, which includes submissions from hundreds of laboratories and clinics worldwide. We analyzed a subset of ClinVar data focused on specific clinical areas and we find high reproducibility (>90% concordance) among labs, although challenges for the community are clearly identified in this dataset. We further review results for the commonly tested BRCA1 and BRCA2 genes, which show even higher concordance, although the significant fragmentation of data into different silos presents an ongoing ch...
Organizations such as the American College of Medical Genetics (ACMG) and the National Society of Ge...
In this article, we examine work with communal data in the context of clinical genetic testing. Draw...
Sharing de-identified genetic variant data via custom-built online repositories is essential for the...
Open sharing of clinical genetic data promises to both monitor and eventually improve the reproducib...
Genetic tests of the cancer predisposition genes BRCA1 and BRCA2 inform significant clinical decisio...
Data sharing between laboratories, clinicians, researchers, and patients is essential for improvemen...
International audienceAs next-generation sequencing increases access to human genetic variation, the...
The BRCA Challenge is a long-term data-sharing project initiated within the Global Alliance for Geno...
The BRCA Challenge is a long-term data-sharing project initiated within the Global Alliance for Geno...
Clinical testing of BRCA1 and BRCA2 began over 20 years ago. With the expiration and overturning of ...
The BRCA Challenge is a long-term data-sharing project initiated within the Global Alliance for Geno...
Well-characterized reference materials (RMs) are integral in maintaining clinical laboratory quality...
Access to detailed variant data is key to inform and verify the interpretation of genomic data. Clin...
Background: Increasing use of BRCA1/2 testing for tailoring cancer treatment and extension of testin...
Background: The Canadian Open Genetics Repository is a collaborative effort for the collection, stor...
Organizations such as the American College of Medical Genetics (ACMG) and the National Society of Ge...
In this article, we examine work with communal data in the context of clinical genetic testing. Draw...
Sharing de-identified genetic variant data via custom-built online repositories is essential for the...
Open sharing of clinical genetic data promises to both monitor and eventually improve the reproducib...
Genetic tests of the cancer predisposition genes BRCA1 and BRCA2 inform significant clinical decisio...
Data sharing between laboratories, clinicians, researchers, and patients is essential for improvemen...
International audienceAs next-generation sequencing increases access to human genetic variation, the...
The BRCA Challenge is a long-term data-sharing project initiated within the Global Alliance for Geno...
The BRCA Challenge is a long-term data-sharing project initiated within the Global Alliance for Geno...
Clinical testing of BRCA1 and BRCA2 began over 20 years ago. With the expiration and overturning of ...
The BRCA Challenge is a long-term data-sharing project initiated within the Global Alliance for Geno...
Well-characterized reference materials (RMs) are integral in maintaining clinical laboratory quality...
Access to detailed variant data is key to inform and verify the interpretation of genomic data. Clin...
Background: Increasing use of BRCA1/2 testing for tailoring cancer treatment and extension of testin...
Background: The Canadian Open Genetics Repository is a collaborative effort for the collection, stor...
Organizations such as the American College of Medical Genetics (ACMG) and the National Society of Ge...
In this article, we examine work with communal data in the context of clinical genetic testing. Draw...
Sharing de-identified genetic variant data via custom-built online repositories is essential for the...