CAPABILITIES
New Technologies
We're always adding new services and technologies — which means you can, too. We look forward to working with you!
In Our Labs TODAY!
Illumina NextSeq 1000
Reliable benchtop sequencing for a wide variety of NGS applications. The NextSeq 1000 is an ideal choice for urgent sequencing projects that require lower sequencing throughput. Access XLEAP-SBS chemistry for whole-genome sequencing, single-cell sequencing, amplicon sequencing, and transcriptomics.
Ultima Genomics UG 100
Increase the scalability of your projects with the latest from Ultima Genomics. 200 mm open silicon wafers replace industry standard flow cells, making projects more affordable. A great choice for detecting rare variants, including SNPs and InDels.
LevitasBio LeviCell EOS
Use LevitasBio's groundbreaking Levitation technology to improve single-cell sequencing sample quality — whether cryopreserved, frozen, or barcoded. The EOS system provides improved sequencing outcomes in sample types that are typically more difficult to process.
10x Genomics Visium HD for CytAssist
Get the newest discovery platform, with as low as 2µm resolution, for whole transcriptome spatial analysis for human and mouse. The Visium CytAssist couples spatial and transcript-specific probes to yield a sequenceable library for cell type identification in a spatial context.
NanoString CosMxTM SMI
Explore spatial biology at single-cell resolution when you use the CosMx. High-plex RNA panels (1,000–6,000 targets) detect transcripts across a wide dynamic range, including low expressors.
10x Genomics Chromium X
Chromium X simplifies, automates, and scales single-cell analysis with its proprietary Next Gen technology. Each of these single-cell partitions contains a unique barcode for downstream analysis, allowing researchers to generate millions of single cells. This system ushers in a new standard in flexibility for single cell technology. Coupled with our new Illumina NovaSeq X Plus, the Chromium X brings robust and cost effective scRNAseq and targeted content.
It is now possible to discover previously unattainable biological information when innovative reagent delivery systems are combined with turnkey software analysis tools.
Illumina NovaSeq X Plus
Psomagen is making the LEAP — we're investing in the latest and greatest technology recently announced by Illumina. Our clients will have access to faster and more robust short-read sequencing on the Illumina NovaSeq X series.
XLEAP-SBS™ technology improves on sequencing by synthesis for improved data accuracy and machine performance. Dual flow cells allow for up to 16 Tb output per run — that's 48 genomes per run, or 26 billion reads per flow cell.
Built-in data analysis means we can run multiple applications simultaneously. That means you get your data faster than ever before.
10x Genomics Xenium Analyzer
Spatial biology has arrived at Psomagen - with the addition of 10X Genomics' Xenium Analyzer to our toolbelt! In situ profiling is a powerful platform that lets you assess the relationship between cellular structure and function like never before. With the Xenium Analyzer, gain access to curated or standalone custom panels, powerful visualization software, and an easy-to-follow workflow.
Profile the RNA or protein content of fresh frozen or FFPE samples. Data is processed simultaneously with the assay, and data is delivered in a format compatible with many data analysis platforms.
PacBio Revio
With PacBio's Revio system, long reads, exceptional accuracy, and direct methylation detection can now be complemented with affordability, high throughput, and ease of use. The system has demonstrated applications in genomics, epigenomics, and transcriptomics with exceptional accuracy, with 90% of bases ≥Q30 and median read accuracy ≥Q30.
The Revio can produce 360 Gb of HiFi reads per day, equivalent to 1,300 human whole genomes per year. In a single run, this technology provides small variants, structural variants, repeat expansions, methylation, and haplotype phasing. With four independent stages, the Revio can sequence multiple samples and applications simultaneously.
Whole Plasmid Sequencing
Go further with long-read sequencing at Psomagen! Whole plasmid sequencing explores all of the genetic material in a plasmid, with no primers, a 16 - 24 business hour TAT, and high accuracy.
Improved chemistry and long-read technology make it possible to conduct difficult region sequencing, bacterial and fungal identification, SNPs and primer walking.
