![]() ![]() The quicker unwanted mutations are spotted, the sooner associated diseases can be identified and treated.” “Its cost and time efficiency gives high-throughput NGS sequencing laboratories the chance to use the technology widely for clinical and research clients. ![]() “LightSpeed will allow QDI to maintain its leadership position in data analysis as the market moves away from analyzing a few hundred selected genes to comprehensive genetic testing,” says Sheldon. This enhancement in CLC Genomics secondary analysis software demonstrates QIAGEN’s continued leadership and commitment to targeted growth areas, including WGS and WES. ![]() QIAGEN Digital Insights’ investment in the LightSpeed technology is ideally suited to NGS areas such as neonatal screening for hereditary diseases or large population-genomics studies in which speed and cost are priorities. “Thanks to LightSpeed’s ground-breaking technology, WGS analysis is extremely fast, beats most other FASTQ to VCF workflows on accuracy, uses less power and requires no investments in new hardware or software licenses beyond CLC.” “QIAGEN CLC Genomics Workbench Premium is much faster, more accurate, greener and cheaper than previous data-analysis and visualization solutions,” says Jonathan Sheldon, PhD, senior vice president of QIAGEN Digital Insights. Alternatively, labs can efficiently run the QIAGEN CLC LightSpeed technology on existing local hardware with similar performance. With QIAGEN CLC LightSpeed software accelerator technology, labs can run WGS analyses for about $1 per genome and WES for less than a few cents per exome using cloud infrastructure, the company says. It can analyze an entire human genome at 34x coverage on an ordinary computer in just 25 minutes and a 50x whole exome in 90 seconds within standard cloud environments. The update to QIAGEN CLC Genomics Workbench Premium incorporates a software accelerator that converts raw sequencing data in FASTQ files from any paired-end short read sequencing platform into interpretable lists of genetic variants in the VCF format. Remember that annotation is optional for genome submissions.QIAGEN Digital Insights (QDI), the bioinformatics business of QIAGEN, unveiled their enhanced QIAGEN CLC Genomics Workbench Premium that removes the data-analysis bottleneck of next-generation sequencing (NGS) via improved analysis speed to help analyze and interpret whole genome sequencing (WGS), whole exome sequencing (WES), and large panel sequencing data. Provide these preregistered BioProject and BioSample accessions in the genome submission. Do not register a duplicate BioProject or BioSample for the same genome. Write to if you did not receive a locus_tag prefix. Wait for the installation process to complete, choose whether you would like to launch CLC Sequence Viewer right away, and click Finish. If you check this option, double-clicking a file with a “clc” extension will open the CLC Sequence Viewer. The MacOS package is an executable disk image.Ĭlc files to CLC Sequence Viewer. Windows 10 (64-bit) The Windows 10 package is a native Windows installer.Please download Genome Workbench version for your system from the Downloads page. The software for either platform can be downloaded from. The CLC Sequence Viewer is developed for Windows, Mac OS X and Linux. Genome Workbench is an application that you can download to your computer that allows you to view and analyze sequence data. The CLC Genomics Workbench is developed for Windows, Mac OS X and Linux. How do I download CLC Genomics Workbench? CLC Free Workbench is fully integrated with all commercial products from CLC bio. QIAGEN CLC Genomics Server is a multi-user, enterprise solution for high throughput sequencing analysis, designed for use on a central compute cluster or server.ĭownload and use is absolutely free of charge. It can also be used to view some of the analysis outputs of CLC commercial workbenches, with the exceptions of some more advanced data types, such as track-based data, and data stored on a CLC Genomics Server. Cutting-edge technology and unique features and algorithms widely used by scientific leaders in industry and academia make it easy to overcome challenges associated with data analysis.ĬLC Sequence Viewer is a free, user friendly application offering access to basic bioinformatics analyses. QIAGEN CLC Genomics Workbench is a powerful solution that works for everyone, no matter the workflow. ![]()
0 Comments
Leave a Reply. |