Corrigendum to Exploring the potential benefits of stratified false discovery rates for region-based testing of association with rare genetic variation [Front. Genet., 5, (2014) 11] DOI: 10.3389/fgene.2014.00011;Exploring the potential benefits of stratified false discovery rates for region-based testing of association with rare genetic variation

Frontiers in Genetics

Volumn 5, Issue JAN, 2014, Pages

  Xu, Chang Jiang ^a,b   Ciampi, Antonio ^b   Greenwood, Celia M T ^a,b  

^a MCGILL UNIVERSITY   (Canada)

^b MCGILL UNIVERSITY   (Canada)

Author keywords

False discovery rate; Genomic annotation; Multiple testing; Rare genetic variants; SNV; Stratified false discovery rate; Whole genome sequencing; Window based tests; Acknowledgments; False discovery rates; Rare genetic variation; Region based tests; UK10k

Indexed keywords

ARTICLE; CHROMOSOME 3; COMPUTER ANALYSIS; DATA PROCESSING; GENE LINKAGE DISEQUILIBRIUM; GENE SEQUENCE; GENETIC ASSOCIATION; GENETIC TRAIT; GENETIC VARIABILITY; KERNEL METHOD; MOLECULAR GENETICS; NONPARAMETRIC TEST; NULL HYPOTHESIS; PHENOTYPIC VARIATION; SIMULATION; STATISTICAL DISTRIBUTION; WINDOW BASED ASSOCIATION TEST;

EID: 84893669233     PISSN: None     EISSN: 16648021     Source Type: Journal    
DOI: 10.3389/fgene.2014.00061     Document Type: Erratum

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