Library prep reimagined.Unrivaled simplicity.
NeoPrep Library Prep System.Coming Soon.
The NeoPrep System is designed for the Illumina family of NGS sequencers and makes the market leading TruSeq and Nextera library prep workflows even easier.
Library Prep Reimagined
The NeoPrep system radically simplifies library prep: far fewer steps, fewer opportunities for error, greater reproducibility, and much less hands-on time.
Transformative Technology Made Easy
NeoPrep enables push-button library prep by marrying the precision of digital microfluidics with Illumina’s renowned ease-of-use.
integrated Solutions
NeoPrep, Illumina sequencers, and the BaseSpace environment together provide a seamless workflow from library prep to sequencing to analysis
Versatility to Meet Your Needs
NeoPrep delivers 16 libraries per run, starting from as low as 1 ng of input for some assays. NeoPrep kits will include TruSeq PCR-free, TruSeq Nano, TruSeq Stranded mRNA, TruSeq RNA Access, and other assays from Illumina's industry-leading TruSeq and Nextera portfolio.
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Innovative technologies
At Illumina, our goal is to apply innovative sequencing and array technologies to the analysis of genetic variation and function, making studies possible that were not even imaginable just a few years ago. These studies will help make the realization of personalized medicine possible. With such rapid advances in technology taking place, it is mission critical to have solutions that are not only innovative, but flexible, scalable, and complete with industry-leading support and service.
As a global company that places high value on collaborative interactions, rapid delivery of solutions, and prioritizing the needs of its customers, we strive to meet this challenge. Illumina’s innovative sequencing and array-based solutions for genomic analysis serve as tools for disease research, drug discovery, and the development of molecular tests in clinical labs.
Leading-edge products and services
Illumina has developed a comprehensive line of products that address the scale of experimentation and the breadth of functional analysis required to achieve the goals of molecular medicine. Our offering includes leading-edge solutions for:
SNP genotyping
Copy number variation
Genome sequencing
DNA methylation studies
Transcriptome analysis
Gene expression profiling
Our products and services are used by a broad range of academic, government, pharmaceutical, biotechnology, and other leading institutions around the globe.
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