A tool that integrates OMIM and HapMap-based single- and multi-marker predictors of causal SNPs to report the collection of associated alleles in a whole-genome-typed individual.
A tool for parsing population ancestry of admixed individuals.
A tool for detecting IBD segments in "unrelated individuals".
A tool for detecting association to clusters of IBD segments detected by Germline.
A tool for imputing HLA based on GERMLINE output
A tool for selecting INdividual FOr Sequencing by Total Information Potantial, based on GERMLINE output
A tool for graph visualization of hidden relatedness based on GERMLINE output
A tool for computing and visualizing allelic distortion in tumor SNP data
A tool for designing overlappign pools for variant-carrier identification
A tool for power estimation and design of whole-genome resequencing projects aimed at rare variant associations.
A tool for detecting CNVs from low-pass WGS data.