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Gene Variant Databases
Precisely target the causes of malignancy on a molecular level
Key to precision oncology is the development of expert databases that organize and...
Clinical Summits
Lower the barrier to adopt larger CGP in Dx labs: QIAGEN Expert Talks in US
A two-part event, the Break the Data Bottleneck Summit will explore how small to...
Clinical Summits
Lower the barrier to adopt larger CGP in Dx labs: QIAGEN Expert Talks in Europe
A two-part event, the Break the Data Bottleneck Summit will explore how small to...
QIAGEN IPA
Extracting novel hypotheses and insights from single cell data
Follow us on a journey of single cell data exploration. See how you can Process,...
HSMD
Target discovery through QIAGEN IPA and HSMD
Identifying and studying the genomic characteristics of drug targets and important...
QIAGEN CLC Genomics
RNA-seq and single-cell RNA-seq data analysis
In this 90-minute training, users will learn how to easily analyze RNA-seq and...
QIAGEN CLC Genomics
Single Cell ATAC sequence analysis
scATAC-seq (Single-Cell Assay for Transposase-Accessible Chromatin using sequencing) is...
Gene Variant Databases
Access to real-world data and 2 decades of expert curation
Across oncology applications, from research to molecular testing and pharmaceutical...
Discovery and Research User Group Meetings +
Identifying antimicrobial resistance from Sample to Insight
Antimicrobial resistance (AMR) detection and surveillance is a high priority in...
QIAGEN CLC Genomics
Long-read sequencing analysis in the QIAGEN CLC Genomics Workbench
This tutorial is an introduction to working with the tools in the Long Read Support...
QIAGEN OmicSoft and Biomedical Knowledge Base
Human-certified ‘omics data to power drug discovery
Integrating external and internal ‘omics data is a key element of hypothesis...
Gene Variant Databases
Identify meaningful mutations in somatic tumor testing
From Information Overload to Actionable Insights Precision medicine is transforming...