Next-generation sequencing: A new revolution in molecular diagnostics?

Clinical Chemistry

Volumn 55, Issue 12, 2009, Pages 2088-2092

  Diamandis, Eleftherios P ^a,b   Voelkerding, Karl V ^c,d   Drmanac, Rade ^e,f   Agus, David ^g   McPherson, John ^b,h  

^a UNIVERSITY HEALTH NETWORK   (Canada)

^b UNIVERSITY OF TORONTO   (Canada)

^c UNIVERSITY OF UTAH SCHOOL OF MEDICINE   (United States)

^d ARUP LABORATORIES   (United States)

^e Complete Genomics ^*  (United States)

^f Department of Medicine

^g UNIVERSITY OF SOUTHERN CALIFORNIA   (United States)

^h ONTARIO INSTITUTE FOR CANCER RESEARCH   (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

NUCLEIC ACID;

CANCER DIAGNOSIS; CANCER GENETICS; CHOLESTEROL BLOOD LEVEL; DIAGNOSTIC PROCEDURE; GENE IDENTIFICATION; GENETIC VARIABILITY; GENOME; HIGH THROUGHPUT SCREENING; LIFESTYLE MODIFICATION; MOLECULAR GENETICS; NEWBORN SCREENING; NOTE; NUCLEOTIDE SEQUENCE; PROGNOSIS; PROPHYLAXIS; SINGLE NUCLEOTIDE POLYMORPHISM;

FORECASTING; GENOME, HUMAN; HUMANS; MOLECULAR DIAGNOSTIC TECHNIQUES; SEQUENCE ANALYSIS;

EID: 71749091885     PISSN: 00099147     EISSN: 15308561     Source Type: Journal    
DOI: 10.1373/clinchem.2009.133389     Document Type: Note

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