UG 100™ Specification Sheet

Detection of Minimal Residual Disease with Whole Genome Sequencing and High Accuracy ppmSeq™ on the UG 100™

Whole Genome Sequencing and High-Efficiency Library Preparation for Generating and Detecting Minimal Residual Disease (MRD) Signatures

Germline Whole-Genome Sequencing on the UG 100™

Transcriptome profiling using the Ultima Genomics UG 100™ Sequencer

Enabling single cell RNA-seq at scale on the Ultima Genomics UG 100™ Sequencer

Genome-wide DNA methylation profiling using the Ultima Genomics UG 100™ Sequencer

Whole genome error-corrected sequencing for sensitive circulating tumor DNA cancer monitoring

Cost-efficient whole genome-sequencing using novel mostly natural sequencing-by-synthesis chemistry and open fluidics platform

Mapping information-rich genotype-phenotype landscapes with genome-scale Perturb-seq

Mostly natural sequencing-by-synthesis for scRNA-seq using Ultima sequencing

Ultra high-throughput whole-genome methylation sequencing reveals trajectories in precancerous polyps to early colorectal adenocarcinoma

Advancing cancer genomics with cost-effective whole genome sequencing: somatic variant calling using the UG100 platform

Integration of mostly-natural sequencing by synthesis with multiple single cell and spatial assays: 10X Flex, Visium and immune profiling

An automated high-throughput ATAC-seq assay reveals differential transcription factor dosage response of chromatin accessibility

Germline Short Variants detection from UG100 Sequencing Data

Comprehensive Variant Analysis in Clinical Samples by Cost-Effective Whole Genome Sequencing

Single-cell analysis of CD34-enriched blood cells reveals early prognostic markers of myelodysplastic syndromes

Somatic Variant Calling from UG100 Data Using Deep Learning​

Optimizing the GATK for the Ultima Genomics sequencing platform

An evaluation of the Ultima Genomics sequencing platform: scalable, high-throughput sequencing for low-cost whole genome sequencing

Detection and monitoring of circulating tumor DNA using affordable high depth whole genome sequencing on a new sequencing platform

Successful application of mostly-natural sequencing by synthesis to single cell RNA-seq

High-depth colorectal cancer whole genome methylation sequencing using a novel sequencing method reveals trajectories in disease progression

Cost-efficient whole genome-sequencing using novel mostly natural sequencing-by-synthesis chemistry and open fluidics platform - Supplemental

Detection Of Germline Copy Number Variation From Whole Genome Sequencing On UG100

Adapting Google DeepVariant to Ultima Genomics reads for improved variant calling