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Submitted URL: http://jp.qiagenbioinformatics.com/
Effective URL: https://digitalinsights.qiagen.com/
Submission: On June 15 via manual from PH — Scanned from DE
Effective URL: https://digitalinsights.qiagen.com/
Submission: On June 15 via manual from PH — Scanned from DE
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Text Content
* English * 日本語 * Contact Sales * QIAGEN Webshop * Resellers * MyCLC * Search Search * * Solutions * * Discovery and Research * * Biomarker and Target Discovery * Single-Cell Genomics * Microbial/Metagenomics * Gene Regulation * Data and Pipeline Management * NGS Variant Assessment * SARS-CoV-2 Solutions * * Discovery & Research – Powerful digital insights to help you innovate, integrate and translate scientific results into impactful discoveries. * Clinical NGS Testing * * Oncology * * Solid Tumors * Hematological Malignancies * Hereditary Cancers * Inherited Disorders * * Rare & Undiagnosed Diseases * Carrier Screening * Cardiac Disorders * * Arrhythmias * Cardiomyopathies * Clinical Testing Solutions – Deliver patient-specific reports for any NGS panel in minutes with on-demand, expert-curated content and professional interpretation service... * Pharmaceutical Development * * Biomarker and Indication Selection * Cohort Stratification and CDx Design * Molecular Profiling * Trial Accrual and Drug Market Plans * Custom Drug Development Projects * Pharmaceutical Development – Whether searching for clinically applicable biomarkers, designing a new companion diagnostic (CDx), or honing your study accrual and go-to-m... * Partner Program * QCI Interpret for Oncology – Clinical decision support software powered by augmented molecular intelligence that helps clinical labs not only make faster decisions—but... * QCI Interpret for Hereditary Diseases – Clinical decision support software powered by augmented molecular intelligence that gives clinical labs the best possible chance of solving ... * Know your biomarkers: PRKD1 linked to head and neck cancer? – A new cancer gene, PRKD1, has been identified as defining a subset of head and neck cancers. Learn more about its role in oncogenesis and ac... * Products and Services * * Products Overview * * Discovery Insights Portfolio * * Secondary Analysis * * QIAGEN CLC Workbench Premium * QIAGEN CLC Genomics Workbench * QIAGEN CLC Genome Finishing Module * QIAGEN CLC Microbial Genomics Module * QIAGEN CLC Main Workbench * QIAGEN CLC Module and Plugin Overview * Interpretation and Visualization * * QIAGEN Ingenuity Pathway Analysis * QIAGEN OmicSoft Suite * ‘Omics Databases * * QIAGEN Biomedical Knowledge Base * QIAGEN DiseaseLand * QIAGEN GeneticsLand * QIAGEN OncoLand * QIAGEN Single Сell Land * ATCC Cell Line Land * QIAGEN OmicSoft Land Explorer * Enterprise NGS Solutions * * QIAGEN CLC Genomics Server * CLC Server Command Line Tools * QIAGEN CLC Cloud Module * QIAGEN OmicSoft Suite * NGS Variant Assessment * * QCI Interpret Translational * ANNOVAR * QIAGEN Ingenuity Pathway Analysis * QIAGEN OmicSoft * QIAGEN CLC Genomics * Clinical Insights Portfolio * * NGS Secondary Analysis * * QCI Secondary Analysis (Cloud-Based) * Clinical Interpretation & Reporting * * QCI Interpret for Hereditary Diseases * QCI Interpret for Oncology * QCI Precision Insights * Gene Variant Databases * * COSMIC (Catalogue of Somatic Mutations in Cancer) * HSMD (Human Somatic Mutation Database) * HGMD (Human Gene Mutation Database) * Clinical QKB (Clinical QIAGEN Knowledge Base) * Knowledge and Databases * * QIAGEN Biomedical Knowledge Base * Gene Variant Databases * * COSMIC (Catalogue of Somatic Mutations in Cancer) * HSMD (Human Somatic Mutation Database) * HGMD (Human Gene Mutation Database) * Clinical QKB (Clinical QIAGEN Knowledge Base) * Integrated ‘Omics Data * * QIAGEN DiseaseLand * QIAGEN OncoLand * QIAGEN Single Cell Land * ATCC Cell Line Land * QIAGEN Genetics Solution * Real-World Insights Portfolio * Sample to Insight Solutions * Human Gene Mutations Database (HGMD) – Solve more cases faster, with data you can trust using HGMD Professional, the gold standard for identifying inherited disease-causing mutati... * QIAGEN CLC Genomics Workbench – QIAGEN CLC Genomics Workbench is a powerful solution that works for everyone, no matter the workflow. * Services Overview * * QIAGEN Discovery Bioinformatics Services * Clinical Analysis and Interpretation Services * Pharmaceutical Development Bioinformatic Services * Catalogue of Somatic Mutations in Cancer (COSMIC) – Explore the impact of somatic mutations in human cancer with the world’s largest and most comprehensive resource * QIAGEN IPA – Powerful tools to uncover the significance of data and identify new targets or candidate biomarkers within the context of biological systems * Human Somatic Mutation Database (HSMD) – A new somatic database developed by QIAGEN that contains extensive genomic content relevant to solid tumors and hematological malignancies. * QIAGEN OmicSoft – Powerful cloud-enabled ‘omics GUI, complete NGS analysis workflows and unparalleled curated content for immediate exploration * Resources * * News * * Blog * Press Releases * Science * * Case Studies * Technical Information * Literature Citations * Citation Guidelines * Allele Frequency Community * SARS-CoV-2 Resources * Webinars and Events * Webinar: QIAGEN IPA Deeper Dive: Making most out of user’s core analysis – Jun. 20 – Join us for a deeper dive into the IPA core analysis, covering topics like causal networks, regulator effects, etc., in more detail. * Webinar: De novo assembly, BLAST and genome finishing using QIAGEN CLC Genomics Workbench – Jun. 27 – This webinar will introduce users to the tools available for short reads and long reads de novo assembly in QIAGEN CLC Genomics Workbench. * Webinar: Scale your comprehensive genomic profiling workflow – Jun. 22 – Learn how QCI Interpret for Oncology can help automate and scale a comprehensive genomic profiling workflow. * Support * * Technical Support * * FAQs * Latest Improvements * QIAGEN CLC Tutorials * Product Manuals * Maintenance and Support * Contact Support * Training * * IPA Training * Upcoming Webinars * Webinar Recordings * Technical Information * Downloads * * Product Downloads * Module and Plugin Downloads * Example Data * 3d Graphics Support * System requirements * Licensing * * License transfer * MyCLC * On-demand webinar: Investigation of Somatic and Germline Variants by COSMIC, HGMD and QIAGEN Databases – Identifying and studying actionable variants is of great interest to many investigators. In this webinar, COSMIC, HGMD and QIAGEN database w... * On-demand Webinar: Whole exome sequencing (WES) helps understand exceptional survival in rare sarcoma… – In this webinar, we present a unique case study of a treatment-naïve patient with aggressive metastatic uLMS with multiple pulmonary metast... * On-demand Webinar: CRISPR data analysis and interpretation using QIAGEN IPA and CLC Genomics Workbench – QIAGEN Digital Insights is hosting this 90-minute training focused on analyzing CRISPR high-throughput sequencing data using QIAGEN CLC Geno... * About * * QIAGEN Digital Insights * * About Us * Contact * Careers | QIAGEN Digital Insights * QIAGEN Corporate * * Request a Trial * Product Login * Contact * Shop * * How to Purchase * * Contact Sales * QIAGEN Webshop * Resellers * MyCLC * * Search Search QIAGEN DIGITAL INSIGHTS ADVANCING MOLECULAR INTELLIGENCE FROM BENCH TO BEDSIDE 3 MILLION+ PATIENT TESTS ANALYZED 35,000+ PUBLICATIONS CITED 26 MILLION+ CURATED FINDINGS 5,000+ NEW FINDINGS PER DAY 40+ INTEGRATED DATABASES DELIVERING MOLECULAR INSIGHTS FOR 90,000 CUSTOMERS WORLDWIDE It’s a new era of genomics. To act quickly and confidently, you need access to trusted data and leading-edge technology. QIAGEN Digital Insights is here to help you achieve success. With an unrivalled, superior quality knowledge base powered by augmented molecular intelligence (AMI) and a comprehensive portfolio of bioinformatic software and services, we empower you to put science into meaningful action DANISH NATIONAL GENOME CENTER SELECTS QCI FOR WHOLE-GENOME SEQUENCING IN ONCOLOGY READ PRESS RELEASE NEW ULTRA-FAST NGS SECONDARY ANALYSIS THAT PROCESSES A WHOLE GENOME IN 25 MINUTES READ PRESS RELEASE MUNICH LEUKEMIA LABORATORY SELECTS QCI FOR INTERPRETATION OF SOLID TUMOR TESTING READ PRESS RELEASE VIEW ALL NEWS COMBINING HUMAN AND MACHINE INTELLIGENCE TO POWER MOLECULAR INSIGHTS The content core of our portfolio, the QIAGEN Knowledge Base, is powered by augmented molecular intelligence (AMI). Combining artificial intelligence and human expertise, AMI ensures you have trusted, high-quality molecular intelligence to augment and accelerate your decisions. BIOINFORMATICS SOLUTIONS RESEARCH Analysis and Visualization NGS Variant ASSESSMENT KNOWLEDGE AND DATABASES enterprise ngs solutions SERVICES CLINICAL Secondary ANALYSIS INTERPRETATION AND REPORTING GENE VARIANT DATABASES SERVICES PHARMACEUTICAL BIOMARKER SELECTION cohort stratification MOLECULAR PROFILING TRIAL DESIGN/ACCRUAL CUSTOM DEVELOPMENT HAVE A QUESTION? WE'D LOVE TO HEAR FROM YOU. If you’re interested in our bioinformatic solutions and services, please contact us to learn more. We have over 300 bioinformaticians and scientists ready to help you. Contact Us FOLLOW US * * * * * CONTACT US * * Sample to Insight * © QIAGEN 2013–. All rights reserved * Privacy Policy * Sitemap * Trademarks & Disclaimers * Terms & Conditions