Highlighted videos
QIAGEN OmicSoft and Biomedical Knowledge Base
Checkpoint inhibitors investigation in context of biomarkers, drug targets...
This training will focus on how QIAGEN Omicsoft Studio and IPA can be used to discover new biomarkers,...
HGMD
Expanding Germline and Somatic Variant Knowledge and Interpretation
In this 60-minute webinar, learn how the online resources of the Human Gene Mutation Database (HGMD)...
QIAGEN CLC Genomics
QIAGEN CLC Genomics
Metatranscriptome analysis, annotation and pathways investigations using CLC Genomics Workbench
Using CLC Genomics Workbench, we will go through a pipeline for analyzing...
QIAGEN CLC Genomics
De novo assembly, BLAST and genome finishing using QIAGEN CLC Genomics Workbench
This webinar will introduce users to the tools available for short reads...
QIAGEN CLC Genomics
RNA-seq data analysis and interpretation with QIAGEN CLC Genomics Workbench and Ingenuity Pathway Analysis
In this 90-minute training, users will learn how to easily analyze and...
QIAGEN CLC Genomics
Single-cell RNA-seq data analysis and Interpretation
Slides from this training:...
QIAGEN IPA
QIAGEN IPA
QIAGEN IPA Explorer Training: How to get the most from our virtual biobank of transcriptomic data
Data generation and processing are costly and time-consuming. Work smarter,...
QIAGEN IPA
Somatic variants investigation in critical regulatory pathways
This training will focus on using QIAGEN Ingenuity Pathway analysis (IPA) and...
QIAGEN IPA
IPA Deeper Dive: miRNA investigation using IPA
In this 90-minute training session, you will learn how to identify target...
QIAGEN IPA
Drug repurposing: from large-scale biological data to therapeutics
One of the challenges we are facing today is the high cost and slow pace of...
QIAGEN OmicSoft and Biomedical Knowledge Base
QIAGEN OmicSoft and Biomedical Knowledge Base
Checkpoint inhibitors investigation in context of biomarkers, drug targets and pathways using Omicsoft and Ingenuity Pathway Analysis
This training will focus on how QIAGEN Omicsoft Studio and IPA can be used to...
QIAGEN OmicSoft and Biomedical Knowledge Base
Exploring bevacizumab response in low-grade glioma
See how Dr, Nilson from QIAGEN Digital Insights navigates an interesting...
QIAGEN OmicSoft and Biomedical Knowledge Base
Knowledge graphs and more: Analytics-driven drug discovery using advanced biomedical relationships knowledge
High-quality biomedical relationships knowledge is the cornerstone of modern...
QIAGEN OmicSoft and Biomedical Knowledge Base
Inflammatory Bowel Disease: Drug Target and Biomarker Investigation using QIAGEN OmicSoft
In this 90-minute training using Inflammatory Bowel Disease (IBD) public data...
QCI Secondary Analysis
QCI Secondary Analysis
Cloud based secondary analysis: From FASTQ to VCF in minutes
Ajay Athavale, Ph.D., Senior manager, Clinical services, QIAGEN Digital...
QCI Secondary Analysis
Simplify your NGS secondary analysis workflow to 5 steps
As the rate and volume of raw NGS data generation increases, secondary...
QCI Secondary Analysis
From NGS data to Variant identification and visualization
Cristian Cosentino, Ph.D., Senior Field Bioinformatics Application...
Gene Variant Databases
Gene Variant Databases
Precisely target the causes of malignancy on a molecular level
Key to precision oncology is the development of expert databases that...
Gene Variant Databases
Human vs. AI: Why manual curation is irreplaceable in clinical genomics
Artificial intelligence (AI) is currently a buzzword across almost all...
Gene Variant Databases
Access to real-world data and 2 decades of expert curation
Across oncology applications, from research to molecular testing and...
Gene Variant Databases
Identify meaningful mutations in somatic tumor testing
From Information Overload to Actionable Insights Precision medicine is...
QCI Interpret for Hereditary
QCI Interpret for Hereditary
Solve Every Hereditary Disorder Case for All Types of Mutations
Despite incredible advances in genomics, the NGS data interpretation workflow...
QCI Interpret for Hereditary
Overcoming Challenges of CNV Interpretation
Copy number variant (CNV) analysis has been part of clinical diagnostics for...
QCI Interpret for Hereditary
Increasing the efficiency of diagnostic odysseys
Despite rapid cost reductions in sequencing technologies and an...
QCI Interpret for Oncology
QCI Interpret for Oncology
FASTQ to final report: Ultra-fast workflow for CGP
As our molecular knowledge of cancer continually evolves, a new era in cancer...
QCI Interpret for Oncology
50 to 500 genes: Scale-up to comprehensive genomic profiling
In this webinar, we present a workflow-agnostic, informatics software...
QCI Interpret for Oncology
Comparison of methods in routine somatic diagnostics
Dr. Mattia Schmid from UniLabs, Switzerland compares the methods of molecular...
QCI Interpret for Oncology
Rapid, evidence-based reporting of oncology NGS tests at scale
Competing to offer a comprehensive genomic profiling service for solid or...
日本語 (Japanese)
日本語 (Japanese)
QIAGEN CLC Genomics Workbenchによる解析8 蛋白質の3次構造の表示
蛋白質3次構造のデータベースを用い、変異の位置の蛋白質の3次構造を表示させる方法の説明です。
日本語 (Japanese)
QIAGEN CLC Genomics Workbenchによる解析7 系統樹の作成
コンセンサス配列を用いてアライメントを行い、系統樹を作成する過程の説明です。
日本語 (Japanese)
QIAGEN CLC Genomics Workbenchによる解析6 解析結果の確認
レポート、ゲノムブラウザー等で結果の確認を行います。
日本語 (Japanese)
QIAGEN CLC Genomics Workbenchによる解析5 SARS-CoV-2 解析ワークフローの実行
リード配列のインポート、ワークフローの実行についての説明です。