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" 'Where is the missing heritability?' is a question asked frequently in genetic research. The difficulty seems to come down to the common disease/common variant hypothesis not holding up." » Read more
Analytic Solutions
SNP AnalysisGet the most out of your SNP data with the most complete set of genotype analysis tools. |
Copy Number Variation AnalysisFrom cytogenetics to GWAS, SVS 7 delivers the most powerful CNV analysis tools. |
LD and Haplotype AnalysisPowerful new plotting and analytics capabilities for linkage disequilibrium and haplotypes. |
Genome-Wide AssociationTake GWAS to a new level with unparalleled performance on large-scale data. |
Runs of Homozygosity AnalysisIdentify patterns of extended homozygosity and then run statistical tests for association. |
Family-Based AnalysisCutting-edge analytics for virtually any family study design and ascertainment condition. |
Data ManagementEasily manage data of any size and type on a conventional desktop computer. |
Data Editing and EnrichmentReal-time data editing, manipulation, and enrichment on large-scale data. |
Quality AssuranceA robust toolset for quickly assessing and remedying sample and marker issues. |
Interactive VisualizationExplore data and results with unprecedented whole genome navigation and visualization. |
Scripting and IntegrationInnovate, integrate, and automate with a fully-programmatic Python scripting interface. |
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