ResourceLife Sciences
Streamlining NGS library preparation with Veya's effortless automation
14 Aug 2025Workflows vary widely and many labs must support multiple NGS protocols, including both short- and long-read sequencing for DNA and RNA samples. With fluctuating batch sizes and tightly timed incubation steps, this often results in manual inconsistencies and failed experiments.
Explore Veya®, an automated platform that can accommodate a wide range of multiomics workflows without needing complex reconfiguration. It provides the flexibility needed when running new NGS methods and delivers the consistency and reproducibility science demands.
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Next Generation SequencingNext-generation sequencing (NGS), also known as whole-genome sequencing, high-throughput sequencing and massive parallel sequencing, produces and analyses thousands to millions of nucleotide sequences at once. Sequencing systems operate via varying technologies depending on the manufacturer, including sequencing by synthesis, ligation, pyrosequencing, ion semiconductor and single-molecule real-time sequencing. For NGS, library preparation is paramount to successful sequencing. In this section, explore a range of library preparation kits, from targeted, amplicon-based or hybridization-based kits including epigenomic, transcriptomic and genomic workflows to fragmentation kits. Find the best next-generation sequencing products in our peer-reviewed product directory: compare products, check customer reviews and receive pricing direct from manufacturers.