Effective variant detection by targeted deep sequencing of DNA pools: An example from parkinson's disease

Annals of Human Genetics

Volumn 78, Issue 3, 2014, Pages 243-252

  Pihlstrøm, Lasse ^a   Rengmark, Aina ^a   Bjørnarå, Kari Anne ^b   Toft, Mathias ^a  

^a OSLO UNIVERSITY HOSPITAL   (Norway)

^b Drammen Hospital   (Norway)

Author keywords

Mutation screening; Next generation sequencing; Parkinson's disease; Pooled sequencing; Targeted NGS

Indexed keywords

DJ 1 PROTEIN; DNA; LEUCINE RICH REPEAT KINASE 2;

ALLELE; ARTICLE; AUTOSOMAL DOMINANT INHERITANCE; CONTROLLED STUDY; DNA SEQUENCE; DOMINANT GENE; EXON; GENE FREQUENCY; GENE LOCUS; GENE MUTATION; GENE POOL; GENE SEQUENCE; GENETIC CODE; GENETIC VARIABILITY; GENOME ANALYSIS; GENOTYPE; GENOTYPING TECHNIQUE; HETEROZYGOTE; HUMAN; HUMAN GENETICS; MAJOR CLINICAL STUDY; MUTATIONAL ANALYSIS; NUCLEOTIDE SEQUENCE; PARKINSON DISEASE; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; RESTRICTION SITE; SEQUENCE ANALYSIS; BIOLOGY; GENETICS; HIGH THROUGHPUT SEQUENCING; INFORMATION PROCESSING; MEDICAL GENETICS; PROCEDURES; TRENDS;

COMPUTATIONAL BIOLOGY; DATA COLLECTION; EXONS; GENETIC VARIATION; GENETICS, MEDICAL; HIGH-THROUGHPUT NUCLEOTIDE SEQUENCING; HUMANS; PARKINSON DISEASE;

EID: 84897965966     PISSN: 00034800     EISSN: 14691809     Source Type: Journal    
DOI: 10.1111/ahg.12060     Document Type: Article

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