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Genomic Analysis
Standalone Appliance Products
Low cost, fast and secure solutions
for analysis volumes from:
300 – 50,000 whole exomes per year
100 – 10,000 whole genomes per year
CompStor® Analysis Platform
Standalone appliance, for installations in:
- On-Premise data centers
- Private Cloud data centers, HPCs
Increased data security; maximal privacy
Much lower cost than cloud-based analysis and storage
Very reliable access and fast turnaround
Scales up as analysis volumes increase
Secondary Analysis
The ONLY accelerated secondary analysis solution you will need.
- Short read (NGS) and long read sequencer pipelines (Illumina, MGI, ONT and PacBio). Calls with very high accuracy SNPs, indels, structural variants, CNVs, mitochondrial variants.
- Somatic, Germline pipelines
- Panels, Whole Exome (WES), Whole Genome (WGS)
- GRCh37 and GRCh38 references
- Two variant callers; Broad Institute GATK and OmniTier’s proprietary Novos variant caller
The leading variant interpretation solution
- Causal variant selection on target panels, WES and WGS sequencing
- Fast, automated analysis. Example: WGS vcf file to clinical report in only 7 minutes.
- Single, trio and family rare-disease analysis
- Annotates using over 30 knowledge databases
- Run large cohort, GWAS analysis containing up to 20,000 individual samples
- Create and apply custom knowledge databases
- Target panel analysis from WES and WGS sequencing
Tertiary Analysis
Variant Interpretation
CompStor Spectrum™
Complete end-to-end, secondary and tertiary analysis, integrated standalone appliance
To Learn More, Contact Us