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False Discovery Rates and Copy Number Variation     False discovery rate  multiple testing  grouped hypotheses       font style='font-size:12px;'> 2015/8/20
Copy number changes, the gains and losses of chromosome segments, are a common type of genetic variation among healthy individuals as well as an important feature in tumor genomes. Microarray techno...
Intellectual disability (ID) is a highly heritable mental disease. Especially, the underlying molecular mechanism of non-syndromic intellectual disability (NSID), a subtype of ID with no ...
Copy number variation (CNV) or single nucleotide phlyorphism (SNP) is useful genetic resource to aid in understanding complex phenotypes or deseases susceptibility. Although thousands of CNVs and SNPs...
Alzheimer's disease (AD) is the most common form of dementia defined by loss in memory and cognitive abilities severe enough to interfere significantly with daily life activities. Amnestic mild cognit...
Population forces: Sexual antagonisms, dominant genetic effects Guess: William Rice, 1984, Evolution; Brian Charlseworth et al, 1987, Am Nat Vibranovski M et al, 2009, PLoS Genetics (In press): Stag...

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