Ultima Genomics
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This Poster was presented at ASHG 2026 and outlines benchmarking analysis with the Sentieon hybrid variant caller for small and structural-variant detection using Ultima Genomics short-read sequencing combined with low-depth PacBio or Oxford Nanopore Technologies (ONT) long-read data.

This Poster was presented at ASHG 2026 and outlines features of the latest Solaris 2.0 Max chemistry, including paired-end sequencing capabilities for germline whole-genome sequencing applications.

Specifications for UG200 Series of sequencing platforms.

This application note details the high-accuracy performance of Ultima's sequencing platform for germline whole genome sequencing (WGS). By leveraging the new Solaris 2.0 chemistry and an optimized amplification process, Ultima Genomics delivers superior coverage uniformity and variant calling precision, even in traditionally challenging genomic regions.

This Cell publication from Zhu, R. et al tracks the perturbation of 22 million primary CD4+ T cells from 4 donors, providing a foundational resource and new approaches to decode T cell function and human immune traits.

This BioRxiv publication outlines the Encyclopedia of DNA Elements (ENCODE), a product of more than two decades of systematic interrogation of genome function, representing >16,000 genome-wide experiments.

Calculate how many wafers are needed to sequence your project

Calculate how many wafers are needed to sequence your project

This BioRxiv publication from Rylaarsdam, L.E. et al (Oregon Health and Science University) presents a large-scale single cell methylation atlas of the early postnatal mouse brain on >163,000 cells. The majority of the sequencing was performed across 10 wafers on Ultima's UG 100 platform.

This BioRxiv publication presents the description of the full spectrum of somatic variants and complex rearrangements of an early-passage pancreatic cancer cell line and matched normal tissues. Ultima was used for short read fragment analysis.

This Poster presented by Millberg, L.K., Graham, G., Skidmore, Z.L., Gumm, J., Jacobs, K., , Chesnick, B., Olivares-Amaya, R., McDaniel, T., Jones, S., Singh, A., and Rinaldi, L. from Delfi Diagnostics Inc. and Jaimovich, A., and Helman, E. from Ultima Genomics was presented at AACR 2026 and assesses the technical feasibility of the Ultima Genomics platform for the DELFI-TF test.

D1001122 Updated Applications for 1.9+ software releases Sample sheet details include the change to application-based workflows (ABW) This document provides information for supported applications on the UG 100™ sequencing platform, including sequencing workflow, library construction/conversion information, sample sheet parameters, run QC metrics, and descriptions of application-specific on-platform data analysis.