MR DNA molecular research LP .. is a go to for pac bio sequencing on Sequel. Hi Fi reads, long reads, amplicons of any kind.. metagenomes, genomes, transcriptomes, RNAseq any application for long read sequencing on Sequel IIe stop by the MR DNA website http://www.mrdnalab.com.. shoot them an email and you will get great quality service , great sequencing data at a reasonable price. Fast turnaround and above all friendly knowledgeable service . whether you call or email you are immediately connected with Dr. Scot E Dowd who goes out of his way to help researchers .. We spent hours figuring out what we needed and his thoughtful suggestions and guidance got us where we needed to be .. the data was great .. we even decided to include him on our manuscript because without his help our project would not have made such an impact ..
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thanks so much XN I do try to be helpful and thanks for letting us include your note and blatant kindness
PacBio sequencing technology, renowned for its long-read capabilities and exceptional accuracy, revolutionizes genome sequencing and assembly. At MR DNA, we harness PacBio’s cutting-edge solutions to provide researchers with seamless access to high-quality genomic data. The technology’s ability to generate high-fidelity (HiFi) reads ensures that even the most complex genomes can be assembled with unprecedented precision, making it the gold standard for resolving structural variants, repetitive regions, and large insertions or deletions. http://www.mrdnalab.com
For de novo genome assembly, PacBio excels in delivering contiguous, accurate assemblies without the fragmentation often seen with short-read technologies. This is crucial for exploring genomes with high complexity, such as those of plants, fungi, and eukaryotic microbes. At MR DNA, our expertise with PacBio enables us to assemble genomes with long, continuous reads that preserve the integrity of repetitive sequences and provide comprehensive resolution of large structural features. This approach is essential for creating reference-quality assemblies and unlocking insights into genetic architecture.
MR DNA combines PacBio sequencing with advanced bioinformatics pipelines to deliver end-to-end genome assembly solutions. Our hybrid assembly methods integrate PacBio’s long-read data with complementary short-read technologies like Illumina for maximum accuracy and completeness. These workflows are ideal for projects ranging from microbial genome assembly to large-scale studies involving plant or animal genomes. Whether you’re building a reference genome, resolving complex polyploidy, or uncovering novel genes, MR DNA offers the expertise and technology to achieve your goals. Learn how PacBio sequencing with MR DNA can advance your genomic research at MR DNA.
✅ WordPress Page: “PacBio Sequel IIe Long-Read Sequencing – MR DNA”
Title: PacBio Long-Read Sequencing Services | MR DNA Molecular Research LP
Slug: pacbio-sequel-long-read-sequencing
Meta Title: PacBio Sequel IIe HiFi Long-Read Sequencing | MR DNA
Meta Description: MR DNA is your trusted provider for PacBio long-read sequencing. Get HiFi reads for amplicons, metagenomes, transcriptomes, genomes, and RNAseq with Sequel IIe.
🔬 PacBio Sequel IIe HiFi Long-Read Sequencing – MR DNA Molecular Research LP
Looking for high-accuracy, long-read sequencing for your most challenging genomic projects?
MR DNA Molecular Research LP is your go-to provider for PacBio Sequel IIe sequencing, delivering HiFi reads, full-length amplicons, and long-read solutions for any application.
We offer complete PacBio workflows with expert support — from DNA extraction and library prep to data analysis and interpretation.
🚀 Why Use PacBio at MR DNA?
The Sequel IIe system generates HiFi reads with Q20 (99%+) accuracy, enabling high-resolution insights in:
- ✅ Complex microbiomes and metagenomes
- ✅ Amplicons up to 10–15 kb or longer
- ✅ Whole genomes (bacteria, fungi, viruses, eukaryotes)
- ✅ Isoform-level transcriptomics (Iso-Seq)
- ✅ RNAseq for full-length mRNA profiling
- ✅ Structural variation and repeat resolution
- ✅ Circular consensus sequencing (CCS)
🧬 Applications We Support
MR DNA offers long-read sequencing for a wide range of research fields:
| Application Type | Details |
|---|---|
| Amplicon Sequencing | Any target – 16S, ITS, custom long amplicons |
| Metagenomics | Resolve low-abundance species, complete genomes |
| Whole Genomes | De novo assemblies, large insert scaffolding |
| Transcriptomics | Iso-Seq, RNAseq with full-length isoform capture |
| Microbiome & Virome | Long-read resolution of mixed samples |
⚡ Fast Turnaround + Expert Analysis
- Rapid sequencing and project initiation
- Custom bioinformatics available (assembly, annotation, QC, visualization)
- Clear, publication-ready reports and figures
Whether you’re sequencing bacteria, fungi, viruses, or eukaryotic organisms, we make long-read sequencing simple and effective.
📍 Why Choose MR DNA?
- 🧪 Experienced PacBio service provider
- 📈 HiFi accuracy with long-read resolution
- 🎯 Targeted or shotgun long-read solutions
- 📞 Direct support from expert scientists
- 🌍 Trusted by universities, hospitals, and biotech firms worldwide
📞 Get Started Today
Visit the MR DNA website to learn more or request a quote.
We’re here to help you unlock the power of long-read sequencing for your next discovery.
📧 Email: info@mrdnalab.com
📞 Phone: 1-806-789-7984
👉 Contact Us
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