Clinical Interpretation of Variants from Next-Generation Sequencing: The 2016 Scientific Meeting of the Human Genome Variation Society.

Oetting, William S; Brookes, Anthony J; Béroud, Christophe; Taschner, Peter E

Oetting, William S; Brookes, Anthony J; Béroud, Christophe; Taschner, Peter E.

Affiliation

Oetting WS; Department of Experimental and Clinical Pharmacology, University of Minnesota, Minneapolis, Minnesota. oetti001@umn.edu.
Brookes AJ; Department of Genetics, University of Leicester, Leicester, United Kingdom.
Béroud C; Aix Marseille Universite, Marseille, France.
Taschner PE; Department of Human Genetics, Leiden University Medical Center, Leiden, The Netherlands.

Hum Mutat ; 37(10): 1110-3, 2016 10.

Article in En | MEDLINE | ID: mdl-27492570

Subject(s)

Genetic Variation; High-Throughput Nucleotide Sequencing; Sequence Analysis, DNA; Genetic Predisposition to Disease; Genome, Human; Genomics/ethics; High-Throughput Nucleotide Sequencing/ethics; Humans; Sequence Analysis, DNA/ethics

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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Genetic Variation / Sequence Analysis, DNA / High-Throughput Nucleotide Sequencing Limits: Humans Language: En Journal: Hum Mutat Journal subject: GENETICA MEDICA Year: 2016 Type: Article

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