Note Archive

Probabilistic fine-mapping of transcriptome-wide association studies

A Bayesian approach to mediation analysis predicts 206 causal target genes in Alzheimer’s disease

Twas Egger

Smr Revisit

Coloc

DAP algorithm and DAP-G

PennCNV: An integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data

Genealogical trees, coalescent theory and the analysis of genetic polymorphisms

Reverse Pathway Genetic Approach Identifies Epistasis in Autism Spectrum Disorders

Modeling Linkage Disequilibrium Increases Accuracy of Polygenic Risk Scores

Statistical Epistasis Is a Generic Feature of Gene Regulatory Networks

Resolving the Paradox of Sex and Recombination

Epistasis — the essential role of gene interactions in the structure and evolution of genetic systems

From Peas to Disease: Modifier Genes, Network Resilience, and the Genetics of Health

The background puzzle: how identical mutations in the same gene lead to different disease symptoms

Detecting epistasis in human complex traits

Variance component testing in generalised linear models with random effects

Optimal tests for rare variant effects in sequencing association studies

Score Test

The genetic architecture of type 2 diabetes

Joint Analysis of SNP and Gene Expression Data in Genetic Association Studies of Complex Diseases

Sherlock: Detecting Gene-Disease Associations by Matching Patterns of Expression QTL and GWAS

Conditional and joint multiple-SNP analysis of GWAS summary statistics identifies additional variants influencing complex traits

Mendelian randomization and instrumental variable regression

Integration of summary data from GWAS and eQTL studies predicts complex trait gene targets

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