We work with a wide range of industry-leading organizations to ensure the compatibility of products optimized for use in PacBio workflows. Our partners have been qualified by PacBio scientists to provide seamless integration and support for customers who are just starting out with PacBio sequencing or expanding their current capabilities.
Use the filters on the right to select by application, sequencing platform, or workflow step.
Agilent is a compatible partner for end-to-end targeted sequencing workflows including automation, library prep, and data analysis. Agilent’s Femto Pulse instrument is recommended for accurate generation of large-insert libraries for de novo large genome sequencing projects and other PacBio applications leveraging multi-kilobase read lengths.
Golden Helix has been delivering industry-leading bioinformatics solutions for over a quarter century with thousands of users worldwide. Their software, VarSeq, enables the import and analysis of PacBio HiFi long-read sequencing. This capability facilitates a complete NGS testing suite for research samples with an increased precision and accuracy for variant calling, improved calling of structural variants and CNVs, and higher genomic definition with phasing and short tandem repeat calls.
IDT has evolved as a leading DNA synthesis company to provide genomics solutions across NGS, CRISPR, Synthetic Biology, and PCR, equipping researchers with the right tools when they need them. IDT’s xGen targeted sequencing solution can be combined with the PacBio Kinnex protocol for bulk RNA sequencing.
Qiagen is a multinational provider of automation, library prep, and data analysis. QIAseq xHYB Long Read Panels offer highly specific and sensitive hybrid capture-based target enrichment for long-read sequencing, ensuring complete and uniform coverage across complex genomic regions, including high-GC content and structural variations. These panels are optimized for Revio and Vega PacBio systems to provide high-quality data for accurate and reliable downstream analyses. Their flexibility and customization options allow researchers to tailor experiments to their specific needs and budgets, while an optimized, user-friendly workflow ensures ease of use. Designed to advance cancer research, precision medicine and structural variant analysis, these panels empower scientists with comprehensive, unbiased genomic insights.
Sage Science’s electrophoretic DNA size selection instruments provide user-adjustable DNA size distributions with outstanding rejection of small fragments. Optimally sized SMRTbell® libraries improve HiFi sequencing results, providing better uniformity and higher quality. PacBio recommends three systems for size selection. The BluePippin processes 4 samples with sample inputs up to 5 ug. For higher throughput needs, the PippinHT can process up to 22 samples in a single run. The SageELF (1 or 2 samples per run) fractionates an entire sample into 12 contiguous size bins, provides the most flexibility in sizing, and produces the narrowest size distributions.
seqWell creates scalable genomics technologies that simplify workflows and help scientists to unlock transformative discoveries with sequencing. seqWell technology is focused on a novel, next-generation transposase, TnX, to drive the high-performance needs of tagmentation and advance NGS. seqWell offers a range of library prep products and fragmentation workflows that allow customers to quickly and easily scale their short- and long-read sequencing initiatives.
Thermo Scientific KingFisher purification instruments automate the extraction of DNA, RNA, proteins, and cells. KingFisher instruments provide easy-to-follow protocols that remove manual steps and reduce overall processing time and errors associated with sample preparation while increasing the yield reproducibility of your results compared to the manual workflows. KingFisher instruments are compatible with PacBio Nanobind HT kits.
PacBio has partnered with Twist Bioscience to deliver long-read target enrichment panels. The initial portfolio of products focuses on challenging, medically relevant genes (Dark Genes panel) and pharmacogenomics (Long Read PGx panel). Custom panel capability broadens access to the benefits of long-read HiFi sequencing like accurate variant detection including structural variants and phasing. By partnering with Twist, PacBio can deliver a targeted sequencing solution that is high throughput and cost-effective while also being supported end-to-end.
The LightBench®, powered by Ranger® Technology, is a three-in-one instrument offering automated DNA size selection, fragment length analysis and fluorometrics. It isolates size ranges of target DNA with industry-leading recovery and precision. LightBench® excludes smaller fragments, optimizing long read inputs to deliver increased mean HiFi read lengths and data yields for PacBio sequencing platforms. To support an automated PacBio library prep workflow, the LightBench® can be integrated into 3rd party liquid handling systems thanks to its SiLA 2-compliant API.
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