Deeper insight through expert curated reference dataĬosmosID identifies bacteria, viruses, fungi, and protists, as well as, antibiotic resistance and virulence factors in a whole genome shotgun metagenomic sample. With the use of our curated genome databases and unrivalled sensitivity and specificity (>95%, and >99% respectively) we are unmatched in our ability to detect microorganisms in metagenomic samples. CosmosID gives you fast, accurate and comprehensive analyses of unassembled next generation sequencing reads. With QIAGEN CLC Genomics Workbench 5.5, researchers can transform NGS data into actionable insights that can advance their research and impact human health.CosmosID Plugin for Qiagen CLC Detect microbes in metagenomic samples with confidenceĮxplore your metagenomic samples with CosmosID and QIAGEN Bioinformatics. 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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