-
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
-
HATS - a tool for calling the amplified alleles and constructing the amplified haplotype within called tumor amplicons
-
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.
-
Inference of Modules associated to eQTLs - a tool for constructing modules regulated by eQTLs using gene expression and SNP variation data across multiple individuals.
-
CONDEX - a tool for calling copy number variants from exome sequencing data.
|