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CLC Genomics Workbench is an integrated genomic data processing solution that addresses the data analysis and management issues found in next-generation sequencing (NGS) data analysis. Rapid Genomics Workbench was designed to provide optimal performance for both long and short reads. Features include in-depth file comparison, paired-end handling, read mapping, as well as a variety of base quality control tests. With the new XML format, the program simplifies and visualizes the data for new and existing users, further boosting end-user productivity. Data and configuration management for all project data is also a major feature. As with other Rapid Genome Workbench products, continuous integration and user-friendly metrics have helped the product succeed by quickly gaining the community's trust.
Transposase is the most powerful driver component in this combination. The transposase of Phi29 is superior to the transposase of other DNA transposons such as Hermes and MuDR. In addition to the high efficiency and low sequence homology of the transposase, the properties of transposon vector of Phi29 make the vector more effective and reliable. That is why we decided to use Phi29 for the “Ultra Fast 2.0” vector, the latest improved version of the vector. Only a few weeks ago, we have launched two improved versions of Amplicon vector. After clinching all users, now we are launching the Transposase in “Ultra Fast 2.0” together. We have expected that the “Ultra Fast 2.0” combination is more powerful than the 1st generation phi29-derived Transposase Amplification (TA) vector due to the highly efficient transposases of bacteriophages, thus it is more efficient than the previous version of the vector.
CLC Genomics Workbench is a next-generation sequencing analysis tool for researchers and clinicians worldwide. It allows the creation of complex analyses and experiments from the raw sequencing data.
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