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

CompStor Novos®

Secondary analysis standalone appliance

CompStor Insight®

Tertiary analysis, variant interpretation standalone appliance

To Learn More, Contact Us

USA

3031 Tisch Way

110 Plaza West

San Jose, CA 95128

USA

Email: sales@omnitier.com

SUPPORT

Email: support@omnitier.com