Highlighted videos
QIAGEN OmicSoft and Biomedical Knowledge Base
Gene set enrichment, target validation and Python-based ‘omics data mining
Learn how to take advantage of QIAGEN Biomedical KB-HD, the high-quality, expert-curated biomedical...
QCI Interpret for Oncology
Clinician’s Roundtable: Interpreting genomic test results for precision oncology
You’re invited to attend the 2024 Clinician’s Roundtable, a virtual event where medical directors and...
QIAGEN IPA
QIAGEN IPA
IPA deeper dive: Making most out of user’s core/expression analysis
An Ingenuity Pathway Analysis (IPA) deeper dive into the core analysis (also...
QIAGEN IPA
Investigate biomarkers, drug targets and more with QIAGEN IPA BioProfiler
QIAGEN IPA's BioProfiler feature allows you to explore and filter the details...
QIAGEN IPA
QIAGEN Ingenuity Pathway Analysis (IPA) summer camp Part 3
• Compare different experimental conditions (different ‘omics data,...
QIAGEN IPA
QIAGEN Ingenuity Pathway Analysis (IPA) summer camp Part 2
• Understand the different result types produced (pathways, key regulators,...
QIAGEN CLC Genomics
QIAGEN CLC Genomics
Antimicrobial resistance (AMR) and multi-locus sequence typing (MLST) with QIAGEN CLC Genomics Workbench
You asked, and we’re here to deliver. In this training, we’ll cover how...
QIAGEN CLC Genomics
De novo assembly, BLAST and genome finishing with QIAGEN CLC Genomics Workbench
This webinar will introduce users to the tools available for short reads...
QIAGEN CLC Genomics
Streamline H5N1 and other microbial samples with CLC Genomics Workbench
In this training, you will learn how to analyze viral samples using QIAGEN...
QIAGEN CLC Genomics
Scale up NGS bioinformatics analysis throughput with CLC Genomics Server and Cloud solutions
More and more biopharma and academic groups are looking to process a large...
QIAGEN OmicSoft and Biomedical Knowledge Base
QIAGEN OmicSoft and Biomedical Knowledge Base
Assessing drug safety with QIAGEN Biomedical KB-AI
Are you a healthcare professional, clinical researcher or data scientist...
QIAGEN OmicSoft and Biomedical Knowledge Base
Discoveries from comparing user data with high-quality public genomics data
Discoveries from comparing user data with high-quality public genomics data...
QIAGEN OmicSoft and Biomedical Knowledge Base
Leveraging the QIAGEN Knowledge Graph and causal embeddings for insights into drug repurposing
By connecting diverse entities and relationships, biomedical knowledge graphs...
QIAGEN OmicSoft and Biomedical Knowledge Base
Accelerating drug discovery with comprehensive curated knowledge (Bio-IT talk)
From our talk at BioIT, join QIAGEN Senior Field Application Scientist, Kyle...
日本語 (Japanese)
日本語 (Japanese)
01. QIAGEN OmicSoft チュートリアル1 概要
OmicSoft の概要と製品の種類についての説明です。
日本語 (Japanese)
02. QIAGEN OmicSoftチュートリアル2 起動と Land の選択
起動後、まず最初に利用するLand を選択します。
日本語 (Japanese)
03. QIAGEN OmicSoftチュートリアル3 グループ分け (Y軸の分類）
表示されているグラフのY軸は疾患の種類、喫煙歴等様々なメタデータで分類できます。
日本語 (Japanese)
04. QIAGEN OmicSoftチュートリアル4 遺伝子の検索、サンプルの絞り込み
単一遺伝子の検索、および様々なメタデータでサンプルの絞り込みを行う方法を解説します。
QCI Interpret for Oncology
QCI Interpret for Oncology
Benefits of integrating targeted next-generation sequencing (NGS) panels into molecular diagnostics of solid tumors
Variant detection of multiple genes from a single tumor sample requires...
QCI Interpret for Oncology
Sample to Insight Oncology
Sample to insight solution for any oncology applocation
QCI Interpret for Oncology
Expert panel: Mitigating variability in somatic variant interpretation
Next-generation sequencing (NGS) oncology panels are becoming integral in...
QCI Interpret for Oncology
Clinician’s Roundtable: Interpreting genomic test results for precision oncology
You’re invited to attend the 2024 Clinician’s Roundtable, a virtual event...
Gene Variant Databases
Gene Variant Databases
HGMD Pro in action: Search, curate and classify genetic variants - Session 1
As the use of next-generation sequencing (NGS) in diagnostics increases, so...
Gene Variant Databases
Germline and Somatic Variant Investigation using COSMIC, HGMD and QCI-IT
The accurate identification and annotation of germline and somatic variants...
Gene Variant Databases
Advances in Genomic Testing for Rare Disease Diagnostics
Over the past decade, whole-exome and whole-genome sequencing have...
Gene Variant Databases
Leveraging expert-curated knowledge from COSMIC and QIAGEN to avoid pitfalls, qualify candidate drug targets, and accelerate early discovery
The cancer drug discovery landscape is shifting. While research continues to...
QCI Secondary Analysis
QCI Secondary Analysis
How decentralized and small labs can adopt high-throughput NGS analysis with limited time and resource investment
Next-generation sequencing (NGS) has rapidly gained popularity as a...
QCI Secondary Analysis
Introducing QCI Secondary Analysis
Introducing QCI Secondary Analysis, a new cloud-based service for NGS...