Use of stereotypical mutational motifs to define resolution limits for the ultra-deep resequencing of mitochondrial DNA

European Journal of Human Genetics

Volumn 23, Issue 3, 2015, Pages 413-415

  Gardner, Kristian ^a   Payne, Brendan A I ^a   Horvath, Rita ^a   Chinnery, Patrick F ^a  

^a NEWCASTLE UNIVERSITY   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

BACTERIOPHAGE DNA; MITOCHONDRIAL DNA;

ARTICLE; CONTROLLED STUDY; DNA SEQUENCE; GENE FREQUENCY; GENE MUTATION; GENETIC VARIABILITY; HETEROPLASMY; HUMAN; HUMAN GENOME; LIMIT OF DETECTION; MNGIE SYNDROME; POINT MUTATION; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; STEREOTYPY; CASE CONTROL STUDY; GENETICS; HIGH THROUGHPUT SEQUENCING; INTESTINAL PSEUDO-OBSTRUCTION; MITOCHONDRIAL ENCEPHALOMYOPATHIES; MUTATION; NUCLEOTIDE MOTIF; SENSITIVITY AND SPECIFICITY; STANDARDS;

CASE-CONTROL STUDIES; DNA, MITOCHONDRIAL; HIGH-THROUGHPUT NUCLEOTIDE SEQUENCING; HUMANS; INTESTINAL PSEUDO-OBSTRUCTION; MITOCHONDRIAL ENCEPHALOMYOPATHIES; MUTATION; NUCLEOTIDE MOTIFS; SENSITIVITY AND SPECIFICITY;

EID: 84938420174     PISSN: 10184813     EISSN: 14765438     Source Type: Journal    
DOI: 10.1038/ejhg.2014.96     Document Type: Article

References (8)

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