Software
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MutaGeneSys
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. -
Xplorigin
A tool for parsing population ancestry of admixed individuals. -
Germline
A tool for detecting IBD segments in "unrelated individuals". -
Dash
A tool for detecting association to clusters of IBD segments detected by Germline. -
HLA-IBD
A tool for imputing HLA based on GERMLINE output -
INFOSTIP
A tool for selecting INdividual FOr Sequencing by Total Information Potantial, based on GERMLINE output -
ShareViz
A tool for graph visualization of hidden relatedness based on GERMLINE output -
HaDiT
A tool for computing and visualizing allelic distortion in tumor SNP data -
PoolDesign
A tool for designing overlappign pools for variant-carrier identification -
OPERA
A tool for power estimation and design of whole-genome resequencing projects aimed at rare variant associations. -
Zinfandel
A tool for detecting CNVs from low-pass WGS data.