On combining data from genome-wide association studies to discover disease-associated SNPs (Q908136): Difference between revisions

From MaRDI portal
Added link to MaRDI item.
Set OpenAlex properties.
 
(3 intermediate revisions by 3 users not shown)
Property / MaRDI profile type
 
Property / MaRDI profile type: MaRDI publication profile / rank
 
Normal rank
Property / arXiv ID
 
Property / arXiv ID: 1010.5046 / rank
 
Normal rank
Property / cites work
 
Property / cites work: Genomic Control for Association Studies / rank
 
Normal rank
Property / cites work
 
Property / cites work: Valid Inference in Random Effects Meta‐Analysis / rank
 
Normal rank
Property / cites work
 
Property / cites work: Probability of detecting disease-associated single nucleotide polymorphisms in case-control genome-wide association studies / rank
 
Normal rank
Property / cites work
 
Property / cites work: A systematic comparison of methods for combining \(p\)-values from independent tests / rank
 
Normal rank
Property / cites work
 
Property / cites work: From Genotypes to Genes: Doubling the Sample Size / rank
 
Normal rank
Property / OpenAlex ID
 
Property / OpenAlex ID: W2092706317 / rank
 
Normal rank

Latest revision as of 12:11, 30 July 2024

scientific article
Language Label Description Also known as
English
On combining data from genome-wide association studies to discover disease-associated SNPs
scientific article

    Statements

    On combining data from genome-wide association studies to discover disease-associated SNPs (English)
    0 references
    0 references
    0 references
    0 references
    0 references
    3 February 2016
    0 references
    0 references
    0 references
    0 references
    0 references
    whole genome scans
    0 references
    hypothesis testing
    0 references
    random effects
    0 references
    Wald test
    0 references
    multiple comparison
    0 references
    0 references
    0 references