In this webinar, we’ll introduce algorithms required to perform data analysis for resequencing next-generation sequencing data. Together, we’ll explore: • Read mapper • Variant callers • Annotations and filters • Genome Browser Bring any questions you may have, and we will answer them during the webinar.
The development of new cancer drugs is challenging, costly, and time-consuming. As translational research on cancer diagnostics and genomic profiling rapidly evolves, the ability to confidently and efficiently identify specific oncogenes and tumor suppressors involved in oncogenesis is becoming increasingly difficult. This brief half-hour webinar is intended for biopharmaceutical and biotechnology professionals who need more […]
During this 120-minute training, we’ll teach you how to easily analyze and interpret RNA-seq data using QIAGEN CLC Genomics Workbench and QIAGEN Ingenuity Pathway Analysis (IPA) software. For RNA-seq data, you will learn how to: • Import FASTQ files, cell-matrix files and metadata and how to download references • Map reads to a reference genome and generate gene […]
Join us for a 120-minute training session for new users of QIAGEN IPA. In this training, you’ll learn how to: • Upload your dataset (RNA-seq, scRNA-seq, proteomics, metabolomics and more) and perform interactive core/pathway analysis in IPA • Understand the different result types produced (pathways, key regulators, impact on biological functions/diseases and more) • Compare […]
RNA-seq Analysis Portal, a cloud-based platform you can access from a web browser, helps you analyze your RNA-seq expression data. Its predefined analysis pipelines let you calculate expression levels and identify differential expression and significant pathways, regulators, diseases and functions in just a few steps. The graphical views and interactive plots enable seamless exploration and […]
The clinical interpretation of genetic testing results remains one of the most significant hurdles in effectively applying genomics in modern medicine. Errors in variant interpretation, whether false positives or false negatives, can result in inappropriate medical interventions or missed opportunities for treatment. To mitigate the risks associated with variant misinterpretation, the professional genetics community has […]
If you're a QIAGEN CLC Main and/or Genomics Workbench user, or interested in learning about the below analytics, you won't want to miss this training: • Alignment and tree construction • Sanger sequencing analysis • Cloning and primer design • Other molecular biology tools
Many of you who use QIAGEN Ingenuity Pathway Analysis (IPA) have requested a deeper dive into the IPA core analysis (also known as expression analysis), which is - performed on RNA-seq, scRNA-seq, proteomics and many other types of ‘omics data). You’ve specifically requested to cover topics like causal networks, regulator effects, etc., in more detail. […]
In this webinar, we will present how to analyze RNA-seq data starting from raw sequencing reads. We will touch upon expression analysis, statistical comparison, visualization and functional enrichment of RNA-seq data using an actual dataset and a live demo. During this webinar, we will cover: Mapping of reads to the reference and abundance estimation Principal […]
In this webinar, we will present how to analyze RNA-seq data starting from raw sequencing reads. We will touch upon expression analysis, statistical comparison, visualization and functional enrichment of RNA-seq data using an actual dataset and a live demo. During this webinar, we will cover: Mapping of reads to the reference and abundance estimation Principal […]
QIAGEN CLC Genomics Workbench version 24 is here with exciting updates we'd like to share with you. These include: Our QIAGEN CLC LightSpeed Module which now provides ultrafast somatic workflows Spatial Transcriptomics and ParseBio support in QIAGEN CLC Single Cell Analysis Module Amplicon classification for ONT reads in QIAGEN CLC Microbial Genomics Module New Structural […]
QIAGEN CLC Genomics Workbench version 24 is here with exciting updates we'd like to share with you. These include: Our QIAGEN CLC LightSpeed Module which now provides ultrafast somatic workflows Spatial Transcriptomics and ParseBio support in QIAGEN CLC Single Cell Analysis Module Amplicon classification for ONT reads in QIAGEN CLC Microbial Genomics Module New Structural […]
Industry leaders discuss how to improve the speed, precision and cost-effectiveness of clinical exome testing for newborn screening and rare and undiagnosed diseases Clinical exome testing is revolutionizing the diagnosis […]
Watch NowIn this training, you will learn how to analyze viral samples using QIAGEN CLC Genomics Workbench. This webinar will focus on bioinformatics workflows and data interpretation using H5N1 as an […]
Watch NowMore and more biopharma and academic groups are looking to process a large number of samples simultaneously or for a quicker turnaround time. This webinar will introduce a flexible and […]
Watch NowThere is a strong interest in the scientific community to use public (GEO, SRA, TCGA, LINCS, etc.) omics (RNA-seq, scRNA-seq, microarray, proteomics, etc.) data for a variety of discoveries. This […]
Watch NowYou’re invited to attend the 2024 Clinician’s Roundtable, a virtual event where medical directors and oncologists will discuss how to better interpret genomic test results to tailor treatment strategies for […]
Watch NowIngenuity Pathway Analysis (IPA), currently cited in tens of thousands of publications and used by a large number of biopharmaceutical companies, is backed by QIAGEN Biomedical KB-HD. Accordingly, biomedical relationships […]
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