Efficient study design for next generation sequencing

Genetic Epidemiology

Volumn 35, Issue 4, 2011, Pages 269-277

  Sampson, Joshua ^a   Jacobs, Kevin ^a   Yeager, Meredith ^a   Chanock, Stephen ^a   Chatterjee, Nilanjan ^a  

^a NATIONAL CANCER INSTITUTE   (United States)

Author keywords

Next generation sequencing; Rare variants; Sequencing depth; Study design

Indexed keywords

ALLELE; ARTICLE; COST; GENE SEQUENCE; GENETIC ASSOCIATION; GENETIC VARIABILITY; GENOME; NEXT GENERATION SEQUENCING; POPULATION GENETICS; SEQUENCE ANALYSIS; SINGLE NUCLEOTIDE POLYMORPHISM; DNA SEQUENCE; GENETIC PREDISPOSITION; GENOME-WIDE ASSOCIATION STUDY; HIGH THROUGHPUT SEQUENCING; HUMAN; HUMAN GENOME; METHODOLOGY; PROCEDURES; SAMPLE SIZE;

ALLELES; GENETIC PREDISPOSITION TO DISEASE; GENOME, HUMAN; GENOME-WIDE ASSOCIATION STUDY; HIGH-THROUGHPUT NUCLEOTIDE SEQUENCING; HUMANS; POLYMORPHISM, SINGLE NUCLEOTIDE; RESEARCH DESIGN; SAMPLE SIZE; SEQUENCE ANALYSIS, DNA;

EID: 79959568914     PISSN: 07410395     EISSN: 10982272     Source Type: Journal    
DOI: 10.1002/gepi.20575     Document Type: Article

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