Birs- 18w5154: New Statistical Methods for Family-Based Sequencing Studies
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Title: Correcting for confounding introduced by batch effects and imputation in family-based designs with whole genome sequence data
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Title: A General Framework for Variable Selection in Linear Mixed Models with Applications to Genetic Studies with Structured Populations
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Title: Challenges and new approaches for whole genome analysis in multi-ethnic studies with pedigrees
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Title: Sharing of rare nucleotide and copy number variants in extended multiplex families
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Title: Simulating family studies with whole-exome sequencing of multiple affected relatives
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Title: Inferring allele transmissions in very large genealogies
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Title: Next-generation sequencing studies in founder populations
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Title: Rare variant sharing methods with genealogies
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Title: Whole exome sequencing of affected sister pairs with early onset breast cancer
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Title: Statistical methods for the integration of functional genomics data and whole exome/genome sequencing data for improved gene discovery
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Title: Lessons learned from sequencing under a linkage peak in families with vesicoureteric reflux
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Title: Estimating the effects of copy number variants on intelligence quotient using hierarchical Bayesian models
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Title: What's under those old linkage peaks? Combining family and cohort analyses to overcome the limitations of large shared segments
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Title: Using populations and pedigrees structures to identify genetic variations associated with epilepsy
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Title: Joint modelling of family and case controls through mixtures
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Title: Combining phenotypes, genotypes and gene genealogies to find trait-influencing variants
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Title: Inferences from identity by descent in related individuals: pedigree relationships in conjunction and in contrast
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Title: Using gene genealogies to localize trait-influencing variants in diploid populations
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Title: Construction of coalescent trees on partially fixed pedigrees
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Title: Sampling gene genealogies conditional on genotype data from trios
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