A survey of informatics approaches to whole-exome and whole-genome clinical reporting in the electronic health record

Genetics in Medicine

Volumn 15, Issue 10, 2013, Pages 824-832

  Tarczy Hornoch, Peter ^a,b   Amendola, Laura ^a,b   Aronson, Samuel J ^a,c   Garraway, Levi ^a,d,e   Gray, Stacy ^d,e,f,g   Grundmeier, Robert W ^a,e   Hindorff, Lucia A ^a,c   Jarvik, Gail ^b   Karavite, Dean ^a   Lebo, Matthew ^c,e,h   Plon, Sharon E ^a,i   Van Allen, Eliezer ^a,d,f   Weck, Karen E ^a,j   White, Peter S ^a,e   Yang, Yaping ⁱ  

^a NATIONAL HUMAN GENOME RESEARCH INSTITUTE   (United States)

^b UNIVERSITY OF WASHINGTON   (United States)

^c LABORATORY FOR MOLECULAR MEDICINE   (United States)

^d DANA FARBER CANCER INSTITUTE   (United States)

^e HARVARD MEDICAL SCHOOL   (United States)

^f BROAD INSTITUTE OF MIT AND HARVARD   (United States)

^g CHILDREN S HOSPITAL OF PHILADELPHIA   (United States)

^h BRIGHAM AND WOMEN S HOSPITAL   (United States)

ⁱ BAYLOR COLLEGE OF MEDICINE   (United States)

^j UNIVERSITY OF NORTH CAROLINA   (United States)

more..

Author keywords

clinical decision support; clinical sequencing; decision support rules; electronic health record; electronic medical record; next generation sequencing

Indexed keywords

ARTICLE; BIOINFORMATICS; DECISION SUPPORT SYSTEM; ELECTRONIC MEDICAL RECORD; EXOME; GENE FREQUENCY; GENE MUTATION; GENE SEQUENCE; GENOME; HUMAN; INCIDENTAL FINDING; MOLECULAR GENETICS;

DECISION SUPPORT SYSTEMS, CLINICAL; ELECTRONIC HEALTH RECORDS; EXOME; GENOME, HUMAN; HEALTH SURVEYS; HIGH-THROUGHPUT NUCLEOTIDE SEQUENCING; HUMANS; MEDICAL INFORMATICS; NATIONAL INSTITUTES OF HEALTH (U.S.); SEQUENCE ANALYSIS; UNITED STATES; WORKFLOW;

EID: 84885143916     PISSN: 10983600     EISSN: 15300366     Source Type: Journal    
DOI: 10.1038/gim.2013.120     Document Type: Article

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