Secondary findings in 421 whole exome-sequenced Chinese children

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Secondary findings in 421 whole exome-sequenced Chinese children

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wetenschappelijk artikel

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наукова стаття, опублікована у вересні 2018

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Secondary findings in 421 whole exome-sequenced Chinese children

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Secondary findings in 421 whole exome-sequenced Chinese children

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Secondary findings in 421 whole exome-sequenced Chinese children

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Secondary findings in 421 whole exome-sequenced Chinese children

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Secondary findings in 421 whole exome-sequenced Chinese children

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Secondary findings in 421 whole exome-sequenced Chinese children

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P1476

Secondary findings in 421 whole exome-sequenced Chinese children

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Bianmei Han

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Jie Mi

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Kun Zhao

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Meixian Zhang

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Wen Chen

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Wenke Li

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Xuewen Liu

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Yi Ma

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Yuanyuan Fu

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Yujing Zhang

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P2860

Fast and accurate short read alignment with Burrows-Wheeler transform

Analysis of protein-coding genetic variation in 60,706 humans

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

Actionable exomic incidental findings in 6503 participants: challenges of variant classification

The implications of familial incidental findings from exome sequencing: the NIH Undiagnosed Diseases Program experience

Genic intolerance to functional variation and the interpretation of personal genomes

Ethical and policy issues in genetic testing and screening of children.

Technical report: Ethical and policy issues in genetic testing and screening of children.

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.

Assessment of incidental findings in 232 whole-exome sequences from the Baylor-Hopkins Center for Mendelian Genomics

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s40246-018-0174-2

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scholarly article

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10.1186/S40246-018-0174-2

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English

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2018-09-14T00:00:00Z

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1106947594

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30217213

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6137878

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