![]() QIAGEN Digital Insights’ licensing models enable laboratories to analyze WGS and WES samples in parallel. The quicker unwanted mutations are spotted, the sooner associated diseases can be identified and treated.” It is easy to overcome data analysis challenges with cutting-edge. “Its cost and time efficiency gives high-throughput NGS sequencing laboratories the chance to use the technology widely for clinical and research clients. The QIAGEN CLC Geneomics Workbench is a powerful tool that works for all workflows. “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. CLC Genomics Workbench 23.0.4 is for research purposes only. Understand management of reference dataģ.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. Welcome to CLC Genomics Workbench 23.0.4 - a software package supporting your daily bioinformatics work. Learn to work with reads from various platforms (Illumina, IonTorrent, Oxford Nanopore, Pacific Biosciences, BGI/MGI)Ģ. Learn about: Working with reads from various platforms (Illumina, IonTorrent, Oxford Nanopore, Pacific Biosciences, BGI/MGI) Tailored solutions for RNA-seq, DNA-seq and methylation Efficient algorithms for read trimming, mapping, de novo assembly and variant calling Effective management of reference data Scalable processing of many samples, with advanced workflow and reporting capabilities Easy installation on Windows, Mac and Linux.ġ. Qiagens unique protocols and molecular indexing strategies allow for highly complex libraries with minimal bias or sequencing errors to ensure the most. ![]() In this live webinar, Leif Schauser, Ph.D., Director Product Management Genome Analysis, will review a host of new features in the latest release of the QIAGEN CLC Genomics Workbench 20 that help you scale your research, and allow you to ramp up your productivity by taking your multi-sample analyses to the next level. Qiagen Informatics Workbench CLC Genomics Workbench CLC Genomics Workbench is designed to solve the data analysis challenges of high-throughput sequencing with. Powered by cutting-edge technology and accelerated algorithms, it supports a comprehensive set of NGS data analysis applications. Includes maintenance, upgrade and service. 1 year subscription for a static license to use the software on a single computer. This product is not intended for the diagnosis, prevention, or treatment of a disease. QIAGEN CLC Genomics Workbench is a powerful solution to analyze and visualize next generation sequencing (NGS) data. The QIAGEN CLC Workbench Modules is intended for molecular biology applications.
0 Comments
Leave a Reply. |
AuthorWrite something about yourself. No need to be fancy, just an overview. ArchivesCategories |