EXCITING NEWS!

We’ve Acquired BioEcho Life Sciences! Explore Innovative Nucleic Acid Extraction Solutions:

Over 400 NovaSeq X Plus Runs Completed

Run your next project on the NovaSeq X Plus

Admera Health continue to advance our sequencing capabilities with the new Novaseq X Plus to provide outstanding services.

Sequence pre-made libraries with our high-throughput capabilities

Sequencing Only

Explore Our Suite of NGS Sequencers

Researchers looking for sequencing only solutions will find that Admera Health offers a quick and supportive team to reach your goals.

Admera Health works with both individually-barcoded libraries or pre-pooled libraries.

Admera Health uses the MiSeq for your research project needs.

  • v2 1x50

    v3 2x75

    Micro 2x150

    Nano 2x150

    v2 2x150

    Nano 2x250

    v2 2x250

    v3 2x300

  • Mid Output 2x75

    Mid Output 2x150

    Mid Output 2x250

    Mid Output 2x300

    High Output 1x75

    High Output 2x75

    High Output 2x150

    High Output 2x250

    High Output 2x300

  • 10B 2x50

    10B 2x100

    10B 2x150

    25B 2x150

Admera Health uses the NovaSeq for ultra-deep sequencing and delivering the best data for your project

  • SP 2x50

    SP 2x100

    SP 2x150

    SP 2x250

    S1 2x50

    S1 2x100

    S1 2x150

    S2 2x50

    S2 2x100

    S2 2x150

    S4 1x35

    S4 2x100

    S4 2x150

Admera Health uses the PacBio for your long-read research project needs.

  • Sequel I 1M 10 hour

    Sequel I 1M 20 hour

    Sequel I 8M 15 hour

    Sequel II 8M 15 hour

    Sequel II 8M 30 hour

Partial Lane Sequencing

Admera Health is offering partial lane sequencing on the NovaSeq X Plus and NextSeq 1000.

With partial lane sequencing, we can better suit your project’s scale while decreasing costs and turnaround and increasing efficiency.

NovaSeq X Plus 10B
Sequence 10X Libraries

Read length: 2x150

1-25GB:6.66M PE reads to 166M PE reads

25-90GB:166M PE reads to 600M PE reads

>90GB:>600M PE reads

NextSeq 1000
Sequence any Libraries

Read length: 2x300

80M PE reads (40M reads each side)

Connect with a member of our team to get started:

Order a Run on the NovaSeq X Plus

High-Throughput

The NovaSeq X Plus produces maximum throughput and accuracy with up to 8TB of data per flow cell run. 

Cost-Efficient

Get more reads for a low cost per GB. The NovaSeq X Plus generates massive quantities of data that require multiple runs on other platforms to replicate.

Flexible Workflows

Customize your workflow with varying configurations including read lengths and numbers of reads per run to fit your project’s scale.

Connect with us to align your NovaSeq X Plus project:

Advantages of Working with Admera Health

Quick Turnaround Time

Our team operates with urgency to deliver data while maintaining industry leading data quality

Proven Quality Service

Technical & bioinformatic support on sequencing data despite libraries not being constructed in our facilities

High Data Quality

Stringent quality control steps & standard practice to closely monitor all runs to ensure successful delivery

Other NGS Services That Might Be of Interest

Admera Health provides individualized attention for DNA sequencing projects.

Genomics

Admera Health offers exceptional RNA-seq services with flexibility and capability for high-throughput according to customers’ needs.

Transcriptomics

Admera Health’s dedicated team of expert bioinformaticians offer comprehensive data analysis services covering genomics, metagenomics, transcriptomics, and epigenomics.

Bioinformatics