Instrument integration and NGS-specific features aid implementation and adoption
A LIMS (laboratory information management system) designed specifically for genomics and optimized for next-generation sequencing (NGS) can help rapidly and accurately manage and interpret sequencing data. High throughput and complex genomic studies—whether done using NGS or other sequencing technologies—call for a LIMS that integrates with other laboratory systems and scales to increased sample volumes.
NGS labs often find that managing and interpreting the sequencing data are where the bottlenecks and challenges lie, rather than cost or lack of technology. Labs nearly everywhere can adopt high-throughput NGS due to lower costs and better access to the technology. Managing and sequencing samples in this type of environment benefits from a LIMS for efficiency and accuracy.
Here are some of the features you should look for when implementing a LIMS for NGS or other complex genomics studies:
Many labs are surprised to learn that investing in a sequencing instrument is only a fraction of what it takes to conduct next-generation sequencing. Other laboratory tools, such as qPCR instruments, robotic liquid handling systems, and nucleic acid quality control and quantitation systems are routine fixtures. Conducting complex genomic, large-scale, or NGS studies becomes more straightforward when you have a LIMS that integrates with these tools, can automate certain laboratory functions, and can initiate other processes or downstream analyses.
BaseSpace Clarity LIMS is specifically designed for genomics labs of all sizes and is optimized for NGS studies. BaseSpace Clarity LIMS helps labs track samples throughout the sequencing workflow, streamline laboratory operations, and get started quickly via integrations with Illumina and other common laboratory instruments.Learn More About BaseSpace Clarity LIMS
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