With High-Throughput Sequencing machines, High
Throughput Sequencing has become accessible to a very large group of researchers. However, data analysis represents a serious bottleneck in NGS pipelines of most R&D departments, which in turn dramatically reduces the Return of Investment of current NGS assets.
CLC Genomics Workbench solves this problem and will enable everyone to rapidly analyze and visualize the huge
amounts of data generated by NGS machines. The userfriendly and intuitive interface essentially takes High-
Throughput Analysis away from hardcore bioinformatics
programmers doing command-line scripts, and hands it
to scientists searching for biological results. Furthermore, the versatile nature of CLC Genomics Workbench allows it to blend seamlessly into existing sequencing analysis workflows, easing implementation and maximizing return on investment.
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