NGS + PacBio = Insight

Advanced long-read sequencing services

with precision insight,

powered by experts

Unleash the Potential of Precision Sequencing

At RTL Genomics, we're committed to advancing genomic research with our team of experienced researchers, custom collaborations, and state-of-the-art technology.

By leveraging the PacBio Sequel IIe, RTL delivers highly accurate, long-read sequencing that unlocks new opportunities for your research and a flexible solution for your unique genomics needs.

Whether you're assembling genomes or exploring metagenomes, the RTL team provides the tech, service, and expertise your projects require.


Explore our suite of long-read services…

✔ Full Length 16S rRNA Gene Sequencing for Bacterial Identification ✔ Bacterial Sequencing
✔ Amplicon Sequencing (ITS coming soon!)
✔ Shotgun Sequencing / Metagenomics
✔ Biostatistics & Bioinformatics
✔ De Novo Gene Assembly

Have something else in mind?
Let us know! We’re happy to help you find the perfect solution.

Why Work with RTL?

RTL is more than a service provider; we’re a partner in your scientific journey. Our team brings years of client experience and deep expertise with Next-Generation DNA Sequencing (NGS) technologies to realize the full potential of your research. Plus, with over 15 years client experience, our team is one of the most experienced practitioners of 16S rRNA gene sequencing methods.

We provide a full range of services, from sample extraction and library preparation to bioinformatics and biostatistics analyses.

We are proud to serve the global life sciences community, from start-ups to Fortune 500 firms to academia – delivering custom solutions that exceed each client’s goals.

Our team sets itself apart via:

  • Access to Clinically Relevant Reference Databases: Drawing on our sister company, MicroGenDX’s, clinical database, we can fine-tune taxonomic resolutions for human, and select veterinary, microbiomes down to the genus and species levels.

  • Cutting-Edge Tech: We utilize the power of the Illumina MiSeq, Illumina NovaSeq 6000, and the PacBio Sequel IIe to offer robust solutions for both short-read and long-read uses, or whatever your research may need.

  • Value-Driven Excellence: Benefit from our highly competitive prices, delivering superior value to you compared to our industry peers. Our focus on value has proudly allowed us to serve a wide range of clients, from universities to government agencies to startups and Fortune 500 companies.

  • 360° Client Support: Our researchers and biostatisticians provide flexible, holistic support, while engaging with your unique processes and requirements.

Experience research, insight, and discovery.

Made easy – with RTL.

Order with Ease

  1. Send Your Order Request. Use the form below to share your name, organization, contact information, and details about your order, including the estimated number of samples (if known).

  2. Speak With Our Team. An RTL lab expert will promptly reach out to confirm your order details and the specific services you require.

  3. Receive Your Quote & Next Steps: We’ll send you a detailed quote along with step-by-step shipping instructions to send your samples to our lab in Lubbock, Texas.

  4. Ship Your Samples. Following the provided instructions, send your samples to us. Once we receive them, we’ll get right to work!

Say Hello to PacBio!

Employing the PacBio Sequel IIe, RTL produces highly accurate, precision long-read sequencing – unlocking a new realm of impactful research opportunities and sequencing applications.

Here’s how RTL + PacBio can take your endeavor to the next level:

  • HiFi Reads: Achieve exceptional accuracy with high-fidelity (HiFi) and redundant reads of up to 25 kb per read, significantly reducing errors with over 99.9% accuracy.

  • Depth of Coverage: Generate up to 450 Gb of high-quality data per SMRT Cell per run to ensure a thorough analysis of even the most challenging genomic regions. Particularly suited for deep genome sequencing, this increased coverage enables detection of rare variants, mutations, and other low-frequency genomic changes.

  • Long Reads: Resolve intricate genomic regions with long reads averaging 15,000 base pairs, with some exceeding well over 100,000 base pairs.

Curious to learn more about PacBio? Check out this PacBio primer below!

The RTL Story

Since 2004, RTL Genomics has been at the forefront of Next-Generation DNA Sequencing (NGS). Working with its sister company, MicroGenDX, RTL’s origins lie in reshaping microbial diagnostics, particularly in human samples.

Since then, RTL has grown to become a pioneering provider of a range of sequencing services, addressing the scientific needs of industry, government, and academic clients. RTL integrates the latest in technology with deep expertise to help clients achieve their diverse research goals.

From its early days to now, RTL’s commitment to advancing scientific discovery and driving client success remains steadfast.