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 new user training
Are you new to QIAGEN Ingenuity Pathway Analysis (IPA) or interested in...
QIAGEN IPA
Understanding Regulator Effects and Interaction Networks in QIAGEN IPA
Not sure what to do with Regulator Effects and Interaction Networks in IPA?...
QIAGEN IPA
IPA RAP Portal DEMO
Take the stress out of data analysis and fast-track your path to gene...
QIAGEN CLC Genomics
QIAGEN CLC Genomics
Get started with QIAGEN CLC Genomics Workbench
Start out strong with QIAGEN CLC Genomics Workbench and follow along with our...
QIAGEN CLC Genomics
Detecting copy number variants with QIAGEN CLC Genomics Workbench
Learn how to use the copy number variant (CNV) detection tool in the QIAGEN...
QIAGEN CLC Genomics
Investigating genomic variants using QIAGEN CLC Genomics Workbench, QCI Interpret-Translational (QCII-T), and Ingenuity Pathway Analysis (IPA)
Discovery of new genes implicated in hereditary diseases or cancer...
QIAGEN OmicSoft and Biomedical Knowledge Base
QIAGEN OmicSoft and Biomedical Knowledge Base
Investigating biomarkers with manually curated RNA-seq expression data
There is a wealth of RNA-seq expression data scattered across public sources...
QIAGEN OmicSoft and Biomedical Knowledge Base
Discovering and investigating gene signatures for biologists and data scientists
Our high-quality, comprehensive databases are designed for biologists, wet...
QIAGEN OmicSoft and Biomedical Knowledge Base
Discover biomarkers, validate targets and identify variants with QDI software
Learn how to leverage solutions from QIAGEN Digital Insights to discover...
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
How to accelerate your clinical reporting workflow for high-throughput oncology NGS testing
As the demand for personalized cancer treatment grows, clinical diagnostic...
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...
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...
Pharmacogenomic Insights (PGXI)
Pharmacogenomic Insights (PGXI)
A game-changer for pharmacogenomics: One tool to decode drug response to variation in the genome
Each year, more than 134 million patients experience adverse drug events,...