BioQule NGS Solution

BioQule DNA-Seq Library Prep Kit is designed to streamline your Next Generation Sequencing (NGS) workflow by automating DNA library preparation on the BioQule™ NGS System. This kit includes all the essential reagents needed to prepare up to 8 robust DNA libraries, making it an ideal solution for various genomic research applications. The BBioQule DNA-Seq Library Prep Kit uses enzymatic fragmentation and other optimized processes to ensure robust performance, reliable coverage, and minimal sequencing bias. This kit is specifically tailored for Illumina® sequencing platforms and is compatible with a wide range of sample types, allowing flexibility in your research. With a significant reduction in hands-on time and high reproducibility, the BioQule DNA-Seq Library Prep Kit is a powerful tool for researchers seeking efficiency and accuracy in their sequencing workflows. Please note that barcodes and the BioQule NGS Cartridge (P/N CLS158240) must be purchased separately.

BioQule Oxford Nanopore (ONT) Ligation Accessory Kit is engineered to facilitate the preparation of up to 32 robust DNA libraries using the Oxford Nanopore Ligation Sequencing workflow on the BioQule™ NGS System. This kit ensures robust performance, reliable genome coverage, and streamlined automation, significantly reducing manual intervention.

The BioQule™ Bleed to Read DNA Library Prep Kit enables the preparation of up to 8 uniquely dual-indexed paired-end DNA libraries directly from human whole blood using the BioQule™ NGS System. Streamline your genomic research workflow with minimal hands-on time and ensure robust performance for Illumina® sequencing platforms.

The BioQule Illumina® DNA Prep Accessory kit includes a 384-well plate, plate guides and maps, buffers, dye buffers, and standards, necessary for constructing Illumina DNA libraries on the BioQule™ NGS System. Each accessory set is sufficient for 32 library preparation reactions when used with the Illumina DNA Prep kit from Illumina.

The BioQule™ ClaretBIO® SRSLY™ PicoPlus Accessory kit includes essential components for constructing ClaretBIO SRSLY PicoPlus DNA-seq libraries on the BioQule NGS System.

The BioQule™ WatchMaker® RNA Library Prep Accessory Kit is essential for constructing WatchMaker total RNA libraries on the BioQule NGS System. This kit includes 384-well plates, plate guides and maps, buffers, dye buffers, and standards for library preparation and quantification. When used in conjunction with the WatchMaker RNA Library Prep kit from WatchMaker Genomics, this accessory kit contains all necessary materials to prepare 32 reactions.

The Illumina® DNA PCR-free library prep accessory kit consists of a 384-well plate, plate guides and maps, buffers, dye buffers and standards. This is needed to construct Illumina DNA PCR free libraries on the BioQule™ NGS System. Along with the Illumina DNA PCR-free Library Prep kit, which needs to be purchased from Illumina, this accessory kit contains sufficient material to construct 32 NGS libraries on the BioQule NGS System for sequencing on an Illumina platform.

The BioQule™ NGS – SE Cartridge is a single-use fluid path for mixing and thermocycling bioreactions on the BioQule NGS System.

The BioQule™ NGS Cartridge is a single-use fluid path for mixing and thermocycling bioreactions one the BioQule NGS System.

Revolutionize your NGS workflow with the BioQule™ NGS System. Simplify extraction, library preparation, and quantitation with seamless walk-away automation. This cost-effective, click-and-go solution requires no programming skills, streamlining your process from start to finish. Easy to set up—Simply Pipette, Load, and Go! Our innovative platform offers versatility across diverse applications, allowing you to customize critical parameters to your samples. With automated liquid handling solutions, minimize errors, reduce hands-on time. Coming Soon: BioQule Sample to Seq Workflows – Pathogen to Seq and Cell to Seq Solutions Unlock end-to-end automation for low-throughput genomics! The BioQule™ system simplifies nucleic acid extraction, library preparation, and quantitation, providing fully automated, ready-to-sequence libraries in a single workflow. With specialized applications for Pathogen to Seq and Cell to Seq, labs can effortlessly streamline pathogen detection and single-cell analysis.