This is the first version of documented best practices in sharing and linking phenotypic and genetic data. It identifies and describes best practices on sharing and linking phenotypic and genetic data in both the healthcare sector and in the research setting. The idea is to, as much as possible, avoid reinventing the wheel, learn from previous/current existing projects to improve performance and avoid mistakes made by others
Sharing de-identified genetic variant data is essential for the practice of genomic medicine and is ...
Gaining the trust of patients, healthcare practitioners, research participants and society at large ...
Sharing of genomic and associated data is essential to clinical practice and biomedical research, an...
This is the first version of documented best practices in sharing and linking phenotypic and genetic...
This is the revised first version of documented best practices in sharing and linking phenotypic and...
This is the second version of documented best practices in sharing and linking phenotypic and geneti...
B1MG M3.3 List of best practices in sharing and linking phenotypic and genetic dat
The aim of the 1+MG member states initiative with coordination support of the Beyond 1 Million Genom...
The aim of the 1+MG member states initiative with coordination support of the Beyond 1 Million Genom...
Despite great strides in the development and wide acceptance of standards for exchanging structured ...
Minimum set of recommended standards for the analysis and sharing of the genomics dataset for haemat...
Sharing de-identified genetic variant data is essential for the practice of genomic medicine and is ...
Data sharing is increasingly regarded as an ethical and scientific imperative that advances knowledg...
Modern research into the genetic basis of human health and disease is increasingly dominated by high...
Sharing de-identified genetic variant data is essential for the practice of genomic medicine and is ...
Sharing de-identified genetic variant data is essential for the practice of genomic medicine and is ...
Gaining the trust of patients, healthcare practitioners, research participants and society at large ...
Sharing of genomic and associated data is essential to clinical practice and biomedical research, an...
This is the first version of documented best practices in sharing and linking phenotypic and genetic...
This is the revised first version of documented best practices in sharing and linking phenotypic and...
This is the second version of documented best practices in sharing and linking phenotypic and geneti...
B1MG M3.3 List of best practices in sharing and linking phenotypic and genetic dat
The aim of the 1+MG member states initiative with coordination support of the Beyond 1 Million Genom...
The aim of the 1+MG member states initiative with coordination support of the Beyond 1 Million Genom...
Despite great strides in the development and wide acceptance of standards for exchanging structured ...
Minimum set of recommended standards for the analysis and sharing of the genomics dataset for haemat...
Sharing de-identified genetic variant data is essential for the practice of genomic medicine and is ...
Data sharing is increasingly regarded as an ethical and scientific imperative that advances knowledg...
Modern research into the genetic basis of human health and disease is increasingly dominated by high...
Sharing de-identified genetic variant data is essential for the practice of genomic medicine and is ...
Sharing de-identified genetic variant data is essential for the practice of genomic medicine and is ...
Gaining the trust of patients, healthcare practitioners, research participants and society at large ...
Sharing of genomic and associated data is essential to clinical practice and biomedical research, an...