The challenge of analyzing the results of next-generation sequencing in children

Pediatrics

Volumn 137, Issue , 2016, Pages S3-S7

  Thiffault, Isabelle ^a,b   Lantos, John ^a  

^a CHILDREN S MERCY HOSPITAL   (United States)

^b UNIVERSITY OF MISSOURI KANSAS CITY SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CELL DNA; MITOCHONDRIAL DNA;

ANAMNESIS; ARTICLE; BIOTECHNOLOGY; CLINICAL FEATURE; DIAGNOSTIC ACCURACY; DIAGNOSTIC ERROR; DIAGNOSTIC IMAGING; DIAGNOSTIC VALUE; DISEASE CLASSIFICATION; DNA SEQUENCE; EXOME; GENE MUTATION; GENE SEQUENCE; GENETIC DISORDER; GENETIC SCREENING; GENETIC VARIABILITY; GENOME ANALYSIS; GENOMICS; HUMAN; HUMAN GENOME; LABORATORY TEST; MEDICAL EXAMINATION; MEDICAL RESEARCH; NEXT GENERATION SEQUENCING; PATHOGENICITY; PEDIATRICIAN; PHENOTYPE; PHYSICAL EXAMINATION; POPULATION GENETICS; PRIORITY JOURNAL; CHILD; GENETIC PREDISPOSITION; GENETICS; HIGH THROUGHPUT SEQUENCING; PROCEDURES;

CHILD; EXOME; GENETIC PREDISPOSITION TO DISEASE; GENETIC TESTING; GENOME, HUMAN; HIGH-THROUGHPUT NUCLEOTIDE SEQUENCING; HUMANS; SEQUENCE ANALYSIS, DNA;

EID: 84957671944     PISSN: 00314005     EISSN: 10984275     Source Type: Journal    
DOI: 10.1542/peds.2015-3731C     Document Type: Article

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