Highlighted videos
HGMD
Hybrid Variant Interpretation: Combining AI + Expert Curation to Streamline...
As hereditary NGS testing grows more complex, clinical labs must interpret variants with greater speed...
QCI Interpret for Oncology
Real-World Applications of Clinical Metagenomic Sequencing in Cancer and...
Clinical metagenomic next-generation sequencing (mNGS), the comprehensive analysis of microbial and...
QIAGEN IPA
QIAGEN IPA
IPA Interpret: A hands-on workshop
Now, you can access and share the interpretative power of QIAGEN Ingenuity...
QIAGEN IPA
IPA deeper dive miRNA investigation using QIAGEN Ingenuity Pathway Analysis
In this 90-minute training session, you will learn how to identify target...
QIAGEN IPA
From ‘Omics to Insights Part 1: IPA Dataset Prep and Core Analysis Setup
This is the first part of a series on how you can easily turn your ‘omics...
QIAGEN IPA
Multi-omics (metabolomics, proteomics, transcriptomics) analysis using QIAGEN Ingenuity Pathway Analysis
This 90-minute training session will show you how QIAGEN Ingenuity Pathway...
QIAGEN CLC Genomics
QIAGEN CLC Genomics
Long reads analysis using QIAGEN CLC Genomics Workbench
This webinar will introduce you to the Long Read Support plugin for Oxford...
QIAGEN CLC Genomics
Associating metadata with samples in CLC
In this video, we demonstrate the import and association of metadata with...
QIAGEN CLC Genomics
How to view overlapping genes in a Venn Diagram using the synchronized table view in CLC
In this video, we demonstrate how to view details of specific data points in...
QIAGEN CLC Genomics
Introduction to Fork Collections
Starting with CLC version 26, workflow control can be simplified using fork...
QIAGEN OmicSoft and Biomedical Knowledge Base
QIAGEN OmicSoft and Biomedical Knowledge Base
OmicSoft Explorer Hands-on Workshop: Easily search and interpret deeply curated 'omics datasets
This hands-on workshop will cover a highly requested use case using OmicSoft...
QIAGEN OmicSoft and Biomedical Knowledge Base
From targets to treatments: Data-driven drug discovery across therapeutic areas
The early stages of drug development are inherently high-risk; molecule...
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...
QIAGEN OmicSoft and Biomedical Knowledge Base
QIAGEN OmicSoft trainings- 3 part series - Oct 21 (part 2)
In three separate 60-minute trainings, attendees will learn how to use basic...
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
Is it oncogenic? Comparing guidelines and QCI Interpret CDS for cancer variant interpretation
Accurate clinical interpretation of somatic cancer variants is critical for...
QCI Interpret for Oncology
S2I oncology
S2I oncology
QCI Interpret for Oncology
Streamline clinical reporting for high-throughput oncology NGS testing with QCI Interpret One
With the rising demand for personalized cancer treatments, clinical...
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...
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 Interpret for Hereditary
QCI Interpret for Hereditary
Screening 100,000 newborns using whole genome sequencing: The Genomics England Generation Study
In this on-demand recording from ACMG 2024, hear from Dr. David Bick,...
QCI Interpret for Hereditary
QCI Interpret for Hereditary Disorders
Clinical labs face significant challenges in interpreting germline variants...
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...
Cancer Drug Discovery
Cancer Drug Discovery
Single-cell RNA-seq, cell hashing and spatial transcriptomics
In this training, you will learn how to analyze and interpret your own single...
Cancer Drug Discovery
Targeting MUC16 Neoantigens in Pancreatic Cancer: Precision Oncology and Indication Selection
This webinar shows how we enable identification and prioritization of a novel...
Cancer Drug Discovery
Data curation as a key element in successful data science strategy
Learn the 7 habits of effective manual curation that QIAGEN Digital Insights...
Cancer Drug Discovery
Exploring drug response in low-grade glioma
This webinar introduces the Tumor Microenvironment (TME) Pathway in QIAGEN’s...