A low-cost exon capture method suitable for large-scale screening of genetic deafness by the massively-parallel sequencing approach

Genetic Testing and Molecular Biomarkers

Volumn 16, Issue 6, 2012, Pages 536-542

  Tang, Wenxue ^a   Qian, Dong ^a   Ahmad, Shoeb ^a   Mattox, Douglas ^a   Todd, N Wendell ^a   Han, Harrison ^a   Huang, Shouting ^b   Li, Yuhua ^b   Wang, Yunfeng ^a,c   Li, Huawei ^c   Lin, Xi ^a  

^a EMORY UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b Otogenetics Corporation   (United States)

^c FUDAN UNIVERSITY   (China)

Author keywords

[No Author keywords available]

Indexed keywords

COMPLEMENTARY DNA; DNA FRAGMENT; GENOMIC DNA;

AMPLICON; ARTICLE; CLINICAL PRACTICE; CLONE; CONGENITAL DEAFNESS; CONTROLLED STUDY; COST BENEFIT ANALYSIS; DNA HYBRIDIZATION; DNA LIBRARY; DNA SEQUENCE; EXON; GENE MUTATION; GENE SEQUENCE; GENETIC SCREENING; GENOTYPE; HUMAN; HUMAN TISSUE; HYBRIDIZATION; MOLECULAR BIOLOGY; POLYMERASE CHAIN REACTION;

COMPUTATIONAL BIOLOGY; DEAFNESS; EXONS; GENE TARGETING; GENETIC PREDISPOSITION TO DISEASE; GENETIC TESTING; HIGH-THROUGHPUT NUCLEOTIDE SEQUENCING; HUMANS; INFANT, NEWBORN; MASS SCREENING; SEQUENCE ANALYSIS, DNA;

EID: 84863002929     PISSN: 19450265     EISSN: 19450257     Source Type: Journal    
DOI: 10.1089/gtmb.2011.0187     Document Type: Article

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