Highlighted videos
QIAGEN OmicSoft and Biomedical Knowledge Base
Integrating deeply curated omics data with APIs for biomarkers and drug...
This webinar is for data scientists and bioinformaticians who need extensive high-quality omics data...
Gene Variant Databases
Advances in Genomic Testing for Rare Disease Diagnostics
Over the past decade, whole-exome and whole-genome sequencing have transformed the diagnosis of...
QIAGEN CLC Genomics
QIAGEN CLC Genomics
Single Cell RNA-Seq, Cell Hashing, and Spatial Transcriptomics
In this training, you will learn how to analyze and interpret your own single...
QIAGEN CLC Genomics
Workflow construction and customization using QIAGEN CLC Genomics Workbench
Recently we have received some requests from CLC users (as well as CLC...
QIAGEN CLC Genomics
Long reads analysis using QIAGEN CLC Genomics workbench (with new features - 2024)
This webinar will introduce users to the long read support plugin for Oxford...
QIAGEN CLC Genomics
What’s new in QIAGEN CLC Genomics Workbench version 24
QIAGEN CLC Genomics Workbench version 24 is here with exciting updates we'd...
QIAGEN IPA
QIAGEN IPA
Single cell RNA-seq – data upload & analysis in Ingenuity Pathway Analysis (IPA)
This training is generated based on feedback from recent “Single Cell...
QIAGEN IPA
Multi-omics (metabolomics, proteomics, transcriptomics) analysis using QIAGEN Ingenuity Pathway Analysis
This 90-minute training session is about how QIAGEN Ingenuity Pathway...
QIAGEN IPA
Introduction to Analysis Match in IPA - Compare your gene and protein expression data to over 100.000 published experimental data
With all the expression datasets that are available to the public, wouldn’t...
QIAGEN IPA
IPA deeper dive: Making most out of user’s core/expression analysis and new features
Many of you who use QIAGEN Ingenuity Pathway Analysis (IPA) have requested a...
QIAGEN OmicSoft and Biomedical Knowledge Base
QIAGEN OmicSoft and Biomedical Knowledge Base
Integrating deeply curated omics data with APIs for biomarkers and drug target investigation
This webinar is for data scientists and bioinformaticians who need extensive...
QIAGEN OmicSoft and Biomedical Knowledge Base
Gene set enrichment, target validation and more using high quality biomedical literature findings
This 60-minute session will teach you how to effectively use a relationship...
QIAGEN OmicSoft and Biomedical Knowledge Base
ATCC cell line data utilization for cell line selection, validation and other applications
Cancer cell line models have been a cornerstone of cancer research for...
QIAGEN OmicSoft and Biomedical Knowledge Base
Biomarker discovery, target validation, and variant identification using QIAGEN OmicSoft DiseaseLand, Human Gene Mutation Database, and Ingenuity...
In this webinar, users will learn how to leverage solutions from QIAGEN...
QCI Secondary Analysis
QCI Secondary Analysis
Introducing QCI Secondary Analysis
Introducing QCI Secondary Analysis, a new cloud-based service for NGS...
Gene Variant Databases
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...
Gene Variant Databases
Using COSMIC to predict, identify, and avoid mutational consequences of cancer therapies during early drug development and in patients
Whether your lab is researching and developing targeted cancer therapies or...
Gene Variant Databases
Case studies: Real world examples of how labs can use HGMD Professional to mitigate errors in variant interpretation
The clinical interpretation of genetic testing results remains one of the...
QCI Interpret for Hereditary
QCI Interpret for Hereditary
A breakthrough for rare disease: Completing the Clinical exome gap!
In its latest release, QCI Interpret for Hereditary extends its...
QCI Interpret for Hereditary
Shed light on Hereditary Disorders with QCI Interpret
In this webinar, we will demonstrate how QCI Interpret can improve your...
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 Oncology
QCI Interpret for Oncology
Agilent Alissa to QCI Interpret: How can your lab reduce the stress and complexity of transitioning to a new clinical informatics platform?
In 2023, Agilent announced the discontinuation of their Alissa Interpret...
QCI Interpret for Oncology
How to scale-up comprehensive genomic profiling and deliver confident variant interpretations with QCI Interpret for Oncology
As gene panels increase in size, comprehensive genomic profiling and variant...
QCI Interpret for Oncology
Real-World Applications of Clinical Metagenomic Sequencing in Cancer and Infectious Disease Diagnostics
Clinical metagenomic next-generation sequencing (mNGS), the comprehensive...
QCI Interpret for Oncology
Scale your comprehensive genomic profiling workflow with superior automated variant interpretation
Automating and scaling a comprehensive genomic profiling workflow can be a...
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。