User Guide
Introduction | Input data | Input importation | Importing VCF data | Imported VCF data structures | Importing polygenic score data | Importing phenotype data | Creating a BED-formatted coordinate file | Conversion of PGS weight files to a coordinate file in BED format | Merging coordinates from multiple polygenic scores | Input data validation | Polygenic Score Application | Basic usage | combine.vcf.with.pgs | Allele matching | Missing genotype methods | Custom percentiles | Phenotype analysis | Data Visualization | Common plotting arguments | PGS Density | Basic plot | Add phenotypes | PGS Boxplot | PGS Correlation | PGS Percentile Rank | Optional arguments | Case-control analysis | Basic Plot | Binarize Continuous Phenotypes