Points to consider for laboratories reporting results from diagnostic genomic sequencing.

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The Genomics ADvISER: development and usability testing of a decision aid for the selection of incidental sequencing results

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Points to consider for laboratories reporting results from diagnostic genomic sequencing.

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Points to consider for laboratories reporting results from diagnostic genomic sequencing.

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Points to consider for laboratories reporting results from diagnostic genomic sequencing.

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Points to consider for laboratories reporting results from diagnostic genomic sequencing.

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Points to consider for laboratories reporting results from diagnostic genomic sequencing.

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Points to consider for laboratories reporting results from diagnostic genomic sequencing.

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Points to consider for laboratories reporting results from diagnostic genomic sequencing.

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ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing

Whole-genome sequencing in health care. Recommendations of the European Society of Human Genetics.

Whole-genome sequencing in health care: recommendations of the European Society of Human Genetics.

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.

Precision medicine ethics: selected issues and developments in next-generation sequencing, clinical oncology, and ethics.

Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2016 update (ACMG SF v2.0): a policy statement of the American College of Medical Genetics and Genomics.

The clinical application of genome-wide sequencing for monogenic diseases in Canada: Position Statement of the Canadian College of Medical Geneticists.

Is "incidental finding" the best term?: a study of patients' preferences

Best practice guidelines for the use of next-generation sequencing applications in genome diagnostics: a national collaborative study of Dutch genome diagnostic laboratories.

Reporting practices for variants of uncertain significance from next generation sequencing technologies.

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Points to consider for laboratories reporting results from diagnostic genomic sequencing.

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P2860

P2860

Points to consider for laboratories reporting results from diagnostic genomic sequencing.

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