Our Latest
Literature
UG 100™ Specification Sheet
App Note
Detection of Minimal Residual Disease with Whole Genome Sequencing and High Accuracy ppmSeq™ on the UG 100™
App Note
Whole Genome Sequencing and High-Efficiency Library Preparation for Generating and Detecting Minimal Residual Disease (MRD) Signatures
App Note
Germline Whole-Genome Sequencing on the UG 100™
App Note
Transcriptome profiling using the Ultima Genomics UG 100™ Sequencer
App Note
Enabling single cell RNA-seq at scale on the Ultima Genomics UG 100™ Sequencer
App Note
Genome-wide DNA methylation profiling using the Ultima Genomics UG 100™ Sequencer
Publication
Whole genome error-corrected sequencing for sensitive circulating tumor DNA cancer monitoring
Publication
Cost-efficient whole genome-sequencing using novel mostly natural sequencing-by-synthesis chemistry and open fluidics platform
Publication
Mapping information-rich genotype-phenotype landscapes with genome-scale Perturb-seq
Publication
Mostly natural sequencing-by-synthesis for scRNA-seq using Ultima sequencing
Publication
Ultra high-throughput whole-genome methylation sequencing reveals trajectories in precancerous polyps to early colorectal adenocarcinoma
Poster
Advancing cancer genomics with cost-effective whole genome sequencing: somatic variant calling using the UG100 platform
Poster
Integration of mostly-natural sequencing by synthesis with multiple single cell and spatial assays: 10X Flex, Visium and immune profiling
Poster
An automated high-throughput ATAC-seq assay reveals differential transcription factor dosage response of chromatin accessibility
Poster
Germline Short Variants detection from UG100 Sequencing Data
Poster
Comprehensive Variant Analysis in Clinical Samples by Cost-Effective Whole Genome Sequencing
Poster
Single-cell analysis of CD34-enriched blood cells reveals early prognostic markers of myelodysplastic syndromes
Poster
Somatic Variant Calling from UG100 Data Using Deep Learning
Poster
A cost-efficient workflow for large-scale single-cell RNA-seq using combinatorial indexing and mostly-natural sequencing by synthesis
Poster
Novel Sequencing by Synthesis Platform to Greatly Reduce the Cost of Sequencing
Poster
Optimizing the GATK for the Ultima Genomics sequencing platform
Poster
An evaluation of the Ultima Genomics sequencing platform: scalable, high-throughput sequencing for low-cost whole genome sequencing
Poster
Detection and monitoring of circulating tumor DNA using affordable high depth whole genome sequencing on a new sequencing platform
Poster
Successful application of mostly-natural sequencing by synthesis to single cell RNA-seq
Poster
High-depth colorectal cancer whole genome methylation sequencing using a novel sequencing method reveals trajectories in disease progression
Data
Updated standard reference Genome-in-a-Bottle (GIAB) samples HG001-HG007
Data
MRD ppmSeq Data
Data
10x Genomics: 3' scRNA Data
Data
Whole genome methylation standard reference Genome-in-a-Bottle (GIAB) samples HG001/HG002/HG005
Data
SEQC/MAQC-III Consortium Samples (UHRR and HBRR Libraries)
Data
Single Cell Libraries (5' and 3' PBMCs)
Data
Cost-efficient whole genome-sequencing using novel mostly natural sequencing-by-synthesis chemistry and open fluidics platform - Supplemental
White Paper
Adapting Google DeepVariant to Ultima Genomics reads for improved variant calling
Video
Systematic reconstruction of molecular pathway signatures with massively parallel Pertub-seq
Video
Introducing a New Era: Part Per Million Detection Accuracy with ppmSeq
Video
AGBT 2024 Gold Sponsor Workshop