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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.

D1001358 Rev02 Guidance on the features and use of sample sheets when running the UG 100 sequencing platform. Updated to reflect the use of Applications Based Workflows with software version 1.9 or greater

This IDT/Ultima Genomics collaborative poster (Poster 419) introduces a streamlined Enhanced Whole Genome Sequencing (eWGS) workflow that combines the breadth of WGS with the depth of targeted capture in a single, unified process. DNA libraries are prepared using xGen DNA library prep kits (mechanical or enzymatic fragmentation), ligated with xGen HybCap Adapters for Ultima, PCR-amplified with eWGS Conditioning Reagents, then captured with xGen Hyb V3 reagents and sequenced on the UG100 sequencer. The streamlined eWGS workflow is fully compatible with the UG100 platform, supports tunable coverage for diverse panel sizes, and delivers high-quality data for both population genomics and oncology research—identifying large rearrangements alongside low-frequency SNVs in a single, simplified process.

This BioRxiv publication from Bayard, Q. et al (Owkin) provides a comprehensive clinically orientated evaluation of the UG 100, demonstrating its utility in population-scale genomics, and highlighting its potential to lower the cost of biomedical research and clinical diagnostics.

Whole genome germline sequencing (WGS) of seven Genome in a Bottle (GIAB) reference samples (HG001-HG007). PCR-free genomic DNA libraries were prepared using the new Solaris 2.0 library prep and amplification workflow from Ultima Genomics.