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CompStor Novos®
Scalable, high throughput, secondary analysis appliance
for Illumina, MGI, PacBio and Oxford Nanopore Tech sequencers
Welcome to
CompStor Novos®
CompStor Novos® is an accelerated secondary analysis solution for Illumina, MGI, PacBio and Oxford Nanopore Technology whole genome sequencing (WGS) and whole exome sequencing (WES) datasets. It is an easy to use, plug-and-play appliance delivering lower analysis costs and enabling faster time-to-results, for bioinformatics researchers and clinicians.
This product is for research purposes only.
CompStor Novos®
Built-in support for the following analysis workflows:
Sequencer
- Illumina
- BGI/MGI
- PacBio
- Oxford Nanopore Technology
Analysis
- WGS/WES datasets
- Germline analysis
- Somatic analysis
Variant Discovery
- SNPs/Indels
- Structural Variants (SVs)
- Copy Number Variants (CNVs)
- Mitochondrial
CompStor Novos® Benefits
Short read (Illumina, MGI/BGI) and long read (PacBio, Oxford Nanopore Tech) sequencer support
Accelerated, high throughput de novo assembly or reference alignment and variant calling appliance that can be scaled up or down over time to meet workload demands.
Produces both a standard GATK variant list (SNPs, indels) and higher accuracy SNPs, indels, structural variants, copy number variants and mitochondrial calls from OmniTier’s proprietary Novos® variant caller .
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