This provides complete choice on the client-side of the system, including an option to design your own client. All are built on our service-oriented SOAP web-services. Performance Multiple client options CLC Genomics Server comes with three client options: CLC Genomics Workbench, CLC Server Command Line Tools, and a web interface. CLC Genomics Server is an advanced, high-throughput sequencing focused, three-tier solution offering secure, powerful, and flexible bioinformatics computing on a server-architecture located centrally in your organization.įor more information, visit CLC Genomics Server on our QIAGEN Bioinformatics site. Maximum client-flexibility with support for CLC Genomics WorkbenchHighly customizable on both client- and server-side Advanced and customizable data import/export framework Central data storageĬLC Genomics Server offers a unique and stable software architecture core that makes it possible to apply a range of bioinformatics analysis services on high-throughput sequencing data. Central execution platform with flexible queuing system With QIAGEN CLC Genomics Workbench 5.5, researchers can transform NGS data into actionable insights that can advance their research and impact human health.For flexible next-generation sequencing data analysis It also helps researchers to collaborate and share their results with colleagues and stakeholders. It enables researchers to perform comprehensive NGS data analysis in a fast, accurate, and user-friendly way. QIAGEN CLC Genomics Workbench 5.5 is more than just a software, it is a solution that empowers researchers to discover new insights from NGS data. Moreover, users can integrate QIAGEN CLC Genomics Workbench 5.5 with other QIAGEN products and services, such as QIAGEN Sample to Insight solutions, QIAGEN Clinical Insight, and QIAGEN Discovery Bioinformatics Services. Users can also create their own plugins and tools using the QIAGEN CLC Developer Kit. Users can access a wide range of plugins and tools that are developed by QIAGEN or by third-party developers. QIAGEN CLC Genomics Workbench 5.5 is not only a software, but also a platform that allows users to extend its functionality and customize their workflows. It also supports cloud computing and storage for enhanced scalability and flexibility. It can run on a single computer or on a network of computers, depending on the user's needs and preferences. QIAGEN CLC Genomics Workbench 5.5 is designed to handle large and complex NGS datasets with ease and efficiency. To learn more about QIAGEN CLC Genomics Workbench 5.5, visit It enables researchers to overcome challenges associated with NGS data analysis and to scale their research using cutting-edge technology and unique features. QIAGEN CLC Genomics Workbench 5.5 is a powerful solution that works for everyone, no matter the workflow. Integration with QIAGEN Ingenuity Pathway Analysis for functional interpretation of NGS results.Template workflows for common NGS tasks that can be customized and shared.Biomedical genomics analysis with workflows for hereditary disease and oncology somatic mutation detection.DNA methylation (bisulfite sequencing) analysis with methylation profiling and differential methylation.ChIP-seq analysis with peak detection and motif discovery.RNA-seq analysis with differential expression at gene and transcript levels.Resequencing analysis (WGS, WES, and targeted panel support) with variant calling, annotation, and filtering.Read mapping and de novo assembly of whole genomes and transcriptomes. Some of the features and applications of QIAGEN CLC Genomics Workbench 5.5 include: It also offers an intuitive and user-friendly interface that simplifies data analysis for biologists. It incorporates cutting-edge technology and algorithms that are widely used by scientific leaders in industry and academia. It supports all major NGS platforms, including Oxford Nanopore, PacBio, IonTorrent, BGI/MGI, Illumina, and Sanger. QIAGEN CLC Genomics Workbench 5.5 is a cross-platform desktop software that provides a comprehensive solution for NGS data analysis. However, NGS data analysis can be challenging due to the complexity and volume of the data, as well as the diversity of the applications and workflows. Next-generation sequencing (NGS) is a powerful technology that enables researchers to explore various aspects of genomics, transcriptomics, and epigenomics. QIAGEN CLC Genomics Workbench 5.5: A Comprehensive Solution for NGS Data Analysis
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