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Design of association studies with pooled or un-pooled next-generation sequencing data

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Most common hereditary diseases in humans are complex and multifactorial. Large-scale genome-wide association studies based on SNP genotyping have only identified a small fraction of the heritable variation of these diseases. One explanation may be that many rare variants (a minor allele frequency, MAF
OriginalsprogEngelsk
TidsskriftGenetic Epidemiology
Vol/bind34
Udgave nummer5
Sider (fra-til)479-491
Antal sider13
ISSN0741-0395
DOI
StatusUdgivet - 2010

ID: 35312360