QIAGEN OmicSoft Genetics Solution
A genetics database of biobank-scale genome data to empower genetic disease research
Harnesses the power of large-scale genetics with a custom solution that revolutionizes large genetic data analysis, management and biomedical research.
Understand the mechanisms underlying genetic disease
QIAGEN OmicSoft Genetics Solution harnesses the power of OmicSoft GeneticsLand, a robust genetics database for storing, integrating and querying large-scale genetic datasets for genetic data analysis. It provides an all-in-one solution of curated datasets together with storage, analysis and visualization of genetic data and results, including:
- Data integration via allele standardization (genotype, imputed dose, association result, annotation)
- Phenotype data (numeric, factor, survival and longitudinal)
- Multi-level access controls
- Pre-analysis QC and genotype PCA
- HPC/cloud-enabled parallel analytics
- Interactive data and result visualizations
- Hosted public genetic data and associations
Streamlined data stewardship
Leveraging and integrating with QIAGEN’s bioinformatic tools and pipelines, QIAGEN OmicSoft Genetics Solution with GeneticsLand genetics database provides your organization with a centralized system for the management, analysis and visualization of your internal and collaborative genetic data and public genotype and phenotype data to:
- Save time and resources in gathering and standardizing data for analysis
- Improve collaboration and enable data re-use
- Provide a distributed research and discovery team with fast access to large cross-study data sets
- Automate parallelization of big analyses
Capabilities
QIAGEN OmicSoft Genetics Solution helps you find disease-causing variants faster and with fewer false leads by tapping into our proprietary QIAGEN Knowledge Base. This resource includes a genetics database of curated datasets and knowledge from millions of scientific findings to help you zero-in on causal variants. Capabilities include:
- Biobank-scale fast storage
- Array genotypes (PLINK or VCF)
- Imputed doses (minimac or IMPUTE)
- Sequenced genotypes (VCF)
- Effect allele standardization
- Phenotype data (numeric, factor, survival & longitudinal)
- Multi-level access controls (sample, study, variable)
- Standard exports (VCF or PLINK)
- Pre-analysis QC & genotype PCA
- HPC/cloud-enabled parallel analytics
- Imputation (HAPI-UR/minimac3 or SHAPEIT/IMPUTE2)
- GWAS (linear, logistic, cox)
- Variant annotation (context, frequency, associations, effects)
- SKAT aggregate tests
- Interactive genotype by phenotype visualizations
- Interactive QQ, Manhattan, LocusZoom plots
- Dynamic grouping & filtering
- Pairwise LD
- Germline genotypes and phenotypes from TCGA
- Genetic associations (GRASP and full study results)
Related resources
Brochure
Explore how OmicSoft Genetics Solution can help you reveal the genetic mechanisms of inherited disease
Powerful cloud-enabled ‘omics GUI, complete NGS analysis workflows and unparalleled curated datasets for immediate exploration
QIAGEN Discovery Bioinformatics Services
A reliable and convenient way to extend your in-house resources with tailored bioinformatics ensuring high-quality results
