Analysis of the whole mitochondrial genome: Translation of the Ion Torrent Personal Genome Machine system to the diagnostic bench?

European Journal of Human Genetics

Volumn 23, Issue 1, 2015, Pages 41-48

  Seneca, Sara ^a,b   Vancampenhout, Kim ^b   Van Coster, Rudy ^c   Smet, Joél ^c   Lissens, Willy ^a,b   Vanlander, Arnaud ^c   De Paepe, Boel ^c   Jonckheere, An ^a   Stouffs, Katrien ^a,b   De Meirleir, Linda ^a,b  

^a UNIVERSITY HOSPITAL BRUSSELS   (Belgium)

^b VRIJE UNIVERSITEIT BRUSSEL   (Belgium)

^c GHENT UNIVERSITY HOSPITAL   (Belgium)

Author keywords

[No Author keywords available]

Indexed keywords

GENOMIC DNA;

ALLELE; AMPLICON; ARTICLE; COMPARATIVE STUDY; CONTROLLED STUDY; GENE DELETION; GENE FREQUENCY; GENE INSERTION; HETEROPLASMY; HIGH THROUGHPUT SEQUENCING; HUMAN; INDEL MUTATION; ION TORRENT PERSONAL GENOME MACHINE; LIMIT OF DETECTION; MITOCHONDRIAL GENOME; NEXT GENERATION SEQUENCING; PRIORITY JOURNAL; PSEUDOGENE; REAL TIME POLYMERASE CHAIN REACTION; GENETIC SCREENING; GENETIC VARIATION; GENETICS; GENOMICS; MITOCHONDRIAL DISEASES; PROCEDURES; REPRODUCIBILITY; SENSITIVITY AND SPECIFICITY; STANDARDS;

GENETIC TESTING; GENETIC VARIATION; GENOME, MITOCHONDRIAL; GENOMICS; HIGH-THROUGHPUT NUCLEOTIDE SEQUENCING; HUMANS; MITOCHONDRIAL DISEASES; REPRODUCIBILITY OF RESULTS; SENSITIVITY AND SPECIFICITY; SEQUENCE DELETION;

EID: 84927041444     PISSN: 10184813     EISSN: 14765438     Source Type: Journal    
DOI: 10.1038/ejhg.2014.49     Document Type: Article

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