With today’s next generation sequencing (NGS) technologies, genomics labs can sequence DNA and RNA faster and cheaper than ever before.
As a result of these advanced new technologies, demand for NGS-based tests is escalating, and labs are under increasing pressure to process more samples, at lower costs, and with shorter turnaround times—all without compromising on the high quality needed to ensure confidence in the results.
Many common bottlenecks and quality problems in the NGS workflow can be traced to the laborious and time-consuming task of preparing sequencing-ready libraries.
This guide explains how automating library prep can help improve confidence in the NGS workflow, and what to consider when choosing automation solutions.
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