Ultima Genomics
Ultima Genomics is dedicated to revolutionizing genomics by developing a new sequencing architecture that drives down costs and scales beyond conventional approaches. Their mission is to enable unprecedented advances in biology and human health through scalable, affordable, and high-quality genomic data. They focus on various focus areas including germline, oncology, single-cell sequencing, and proteomics, providing innovative solutions and collaborations to expand the capabilities of genomic research and clinical applications.
Industries
Nr. of Employees
large (251-1000)
Patents
Implementing barriers for controlled environments during sample processing and detection
US-12239980-B2
View DetailsSystems and methods for sequencing error correction via double strand preservation
US-12195797-B2
View Details
Implementing barriers for controlled environments during sample processing and detection
US-12239980-B2
View DetailsSystems and methods for sequencing error correction via double strand preservation
US-12195797-B2
View DetailsProducts
High-capacity wafer-based sequencing platform
A high-throughput NGS instrument architecture based on open-wafer fluidics, flow-based chemistry and integrated on-board compute for primary and secondary analysis; designed to deliver multi-billion reads per wafer and low cost per read/genome.
Library preparation workflows for high-throughput NGS
Collection of validated library preparation workflows including PCR-free whole-genome protocols and flexible indexing PCR workflows that support low-input and existing library conversion for high-throughput sequencing.
Integrated analysis and bioinformatics toolset
Suite of on-board and cloud-compatible secondary analysis pipelines, a flow-optimized aligner, WDL workflow implementations, and containerized tools to support alignment, QC, and variant calling for large-scale datasets.
High-capacity wafer-based sequencing platform
A high-throughput NGS instrument architecture based on open-wafer fluidics, flow-based chemistry and integrated on-board compute for primary and secondary analysis; designed to deliver multi-billion reads per wafer and low cost per read/genome.
Library preparation workflows for high-throughput NGS
Collection of validated library preparation workflows including PCR-free whole-genome protocols and flexible indexing PCR workflows that support low-input and existing library conversion for high-throughput sequencing.
Integrated analysis and bioinformatics toolset
Suite of on-board and cloud-compatible secondary analysis pipelines, a flow-optimized aligner, WDL workflow implementations, and containerized tools to support alignment, QC, and variant calling for large-scale datasets.
Services
Access to high-throughput sequencing through a vetted global network of service providers capable of running high-capacity wafer-based sequencing and delivering processed data.
In-house access to high-capacity sequencers and applications lab with support from consultation through data analysis for researchers who want instrument-level access without purchasing equipment.
Access to high-throughput sequencing through a vetted global network of service providers capable of running high-capacity wafer-based sequencing and delivering processed data.
In-house access to high-capacity sequencers and applications lab with support from consultation through data analysis for researchers who want instrument-level access without purchasing equipment.
Expertise Areas
- High-throughput whole-genome sequencing
- Single-cell sequencing at scale
- Population-scale proteomics sequencing
- Liquid biopsy and minimal residual disease detection
Key Technologies
- Flow-based sequencing chemistry
- Open-wafer fluidics
- Emulsion-based clonal amplification
- Paired‑strand duplex sequencing workflows
News & Updates
Learn how UG 100™ enables genomics at scale at the Santa Fe event.
Participate in talks, posters, and sessions on multiomics sequencing with UG 100™ in Denver.
Explore applications of UG 100™ at the Boston event with workshops, talks, and posters.
A collaboration leveraging AI and NVIDIA GPUs to enable high-quality, low-cost genome sequencing.
A strategic collaboration to develop optimized workflows and reagents for sequencing applications.
A partnership to drive down sequencing costs and develop cancer diagnostic tests.
Learn how UG 100™ enables genomics at scale at the Santa Fe event.
Participate in talks, posters, and sessions on multiomics sequencing with UG 100™ in Denver.
Explore applications of UG 100™ at the Boston event with workshops, talks, and posters.
A collaboration leveraging AI and NVIDIA GPUs to enable high-quality, low-cost genome sequencing.
A strategic collaboration to develop optimized workflows and reagents for sequencing applications.
A partnership to drive down sequencing costs and develop cancer diagnostic tests.