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Ultima Genomics
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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

Direct RNA sequencing of astronaut blood reveals spaceflight-associated m6A increases and hematopoietic transcriptional responses

Nature Communications | Grigorev, K. et al.

Publication

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

bioRxiv | Cheng, A.P., Widman, A.J., Arora, A. et al.

Publication

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

bioRxiv | Almogy, G., Pratt, M., Oberstrass, F. et al.

Publication

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

Cell | Replogle, J.M., Saunders, R.A., Pogson, A.N. et al.

Publication

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

Nature Biotechnology | Simmons, S.K., Lithwick-Yanai, G., Adiconis, X. et al.

Publication

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

bioRxiv | Lee, H., Krieger, G., Clark, T. et al.

Poster

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

AGBT 2024 | Benjamin et. al

Poster

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

AGBT 2024

Poster

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

ASHG 2023 | Liu et al.

Poster

Germline Short Variants detection from UG100 Sequencing Data

ASHG 2023 | Shem-Tov et al.

Poster

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

ASHG 2023 | Pollock et al.

Poster

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

AACR 2023 | Mieri et al.

Poster

Somatic Variant Calling from UG100 Data Using Deep Learning​

AACR 2023 | Shem-Tov et al.

Poster

A cost-efficient workflow for large-scale single-cell RNA-seq using combinatorial indexing and mostly-natural sequencing by synthesis

AGBT 2023 | Jiang et al.

Poster

Novel Sequencing by Synthesis Platform to Greatly Reduce the Cost of Sequencing

Poster

Optimizing the GATK for the Ultima Genomics sequencing platform

AGBT 2022 | Shand et al.

Poster

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

AGBT 2022 | Coole et al.

Poster

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

AGBT 2022 | Rusinek et al.

Poster

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

AGBT 2022 | Simmons et al.

Poster

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

AGBT 2022 | Lee et al.

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

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

White Paper

Adapting Google DeepVariant to Ultima Genomics reads for improved variant calling

Video

Empowering single cell analysis for million cell studies on the UG 100™

Video

Introducing a New Era: Part Per Million Detection Accuracy with ppmSeq

Webinar | Mirna Jarosz & Ariel Jaimovich

Video

Genetics-based Drug Discovery at the Regeneron Genetics Center

AGBT General Meeting - Gold Sponsor Workshop

Video

Systematic reconstruction of molecular pathway signatures with massively parallel Pertub-seq

Video

AGBT 2024 Gold Sponsor Workshop

AGBT 2024 General Meeting | Gilad Almogy & Mirna Jarosz
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