Average Rating: 4.3
2 Scientists have reviewed this product
Ease of use
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Value for money
"Earlier I was working on Genome comparison of bacterial strains. The CLC DNA workbench was useful in annotation and visualization of DNA strands. Primer Designing was also easy to do using the CLC workbench.
In future I will be using the protein workbench along with proteomic tools
08 Jul 2015 | CLC DNA Workbench Software
"This software made analyzing DNA sequences much easier. Instead of having to hardcode or write programs for use, this software does much of the work for you. Additionally, the output images are helpful visualizations of the data."Review date:
01 Feb 2013 | CLC DNA Workbench Software
The New Standard for Desktop-Based Bioinformatics Tools
CLC DNA Workbench provides a software environment which enables users to perform advanced DNA sequence analyses such as assembly of DNA sequence data, graphically and algorithmically advanced primer design, while offering user-friendly molecular cloning tools.
CLC DNA Workbench is a bioinformatics software package containing a range of specialized DNA analyses and bioinformatics tools for molecular biology. It is based on the CLC Free Workbench framework, and has similar work environment, user interface, and framework for graphical viewing. When using CLC DNA Workbench, researchers working in molecular biology labs will be able to do most daily bioinformatics work, including data management and reporting, in one single integrated and user-friendly software package.
CLC DNA Workbench is from the new generation of bioinformatics software - software that also runs on the latest versions of Mac OS X, Windows, and Linux.
Efficient collaboration support
The full compatibility between all types of CLC workbenches provides strong support for efficient collaboration within research groups; advanced analyses and data searches can be performed on a CLC DNA Workbench, while more basic work tasks may be performed by the remaining researchers equipped with CLC Free Workbenches.
Throughout the project, all researchers can be given easy access to knowledge obtained through sharing of sequence data and sharing of research results. Examples could be figures showing annotated sequences, alignments and their underlying sequences, reports on DNA characteristics, phylogenetic trees, BLAST results etc.