Highlighted videos
QIAGEN OmicSoft and Biomedical Knowledge Base
Authenticated and reproducible cell line 'omics data
Have you ever tried to access the genomic profiles of cell lines before using them in your preclinical...
Clinical Summits
Emerging clinical trends in germline NGS testing: Expert Panel Discussion in USA
Hereditary NGS Clinical Summit Series: Build a Next-Gen Software Workflow for Germline Testing Over...
QIAGEN CLC Genomics
QIAGEN CLC Genomics
QIAGEN CLC Main Workbench training
Introduction to QIAGEN CLC Main Workbench • Alignment and tree construction...
QIAGEN CLC Genomics
Understanding and maximising QIAseq secondary analysis in the QIAGEN CLC Genomics Workbench
Join us for a 60 minute training session where attendees will understand how...
QIAGEN CLC Genomics
Multi-locus sequence typing (MLST) using QIAGEN CLC Genomics Workbench
QIAGEN CLC Genomics Workbench Premium provides tools and workflows for a...
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 IPA
QIAGEN IPA
IPA Webinar: Part 3: Search and Explore in IPA
IPA has broadly been adopted by the life science research community and is...
QIAGEN IPA
Single Cell Analysis of the tumor microenvironmnet in High-grade Serous Ovarian Cancer (HGSOC)
Single-cell RNA sequencing (scRNA-seq) is an important technology that...
QIAGEN IPA
IPA Webinar: Part 1: Introduction to Ingenuity Pathway Analysis
Learn how to quickly and easily identify significant pathways, discover...
QIAGEN IPA
IPA Webinar: Part 2: Formatting and Uploading Your Dataset into IPA
IPA has broadly been adopted by the life science research community and is...
QIAGEN OmicSoft and Biomedical Knowledge Base
QIAGEN OmicSoft and Biomedical Knowledge Base
Authenticated and reproducible cell line 'omics data
Have you ever tried to access the genomic profiles of cell lines before using...
QIAGEN OmicSoft and Biomedical Knowledge Base
Investigating public scRNA data using OmicSoft and QIAGEN IPA
Single cell RNA-sequencing (scRNA-seq) has been widely used to investigate...
QIAGEN OmicSoft and Biomedical Knowledge Base
Transforming biological discovery and data science – How direct access to curated data and biological relationships can transform integrated...
In this 90-minute webinar, you will learn more about the range of content...
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。