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QCI Interpret for Hereditary

QCI Interpret for Hereditary Disorders

549 views March 13, 2025

Clinical labs face significant challenges in interpreting germline variants for...

QCI Interpret for Oncology

Streamline clinical reporting for high-throughput oncology NGS testing with...

260 views March 13, 2025

With the rising demand for personalized cancer treatments, clinical diagnostic labs are...

QIAGEN OmicSoft and Biomedical Knowledge Base

Using OmicSoft OncoLand to integrate public expression

404 views March 12, 2025

QIAGEN OmicSoft Lands are high-quality curated repositories of genomics and proteomics...

QIAGEN IPA

Multi-omics (metabolomics, proteomics, transcriptomics) analysis using QIAGEN...

244 views March 03, 2025

This 90-minute training session is about how QIAGEN Ingenuity Pathway Analysis (IPA)...

QCI I Translational

Simplify gene discovery Three solutions to decode variants and pathways

352 views March 03, 2025

Does your lab need a faster and easier way to uncover associations between gene...

HGMD

Decode genetic variants with HGMD Professional

362 views February 28, 2025

Next-generation sequencing (NGS): the technology that took the biological research...

QIAGEN IPA

Deeply curated single-cell RNA-seq data investigation using QIAGEN Omicsoft...

196 views February 27, 2025

Single-cell RNA-sequencing (scRNA-seq) is widely used to investigate tissue...

QIAGEN OmicSoft and Biomedical Knowledge Base

Biomarkers and drug target investigation using manually curated, unified...

228 views February 18, 2025

There is an almost incomprehensible amount of diverse, non-standardized ‘omics data...

QIAGEN OmicSoft and Biomedical Knowledge Base

Mining curated knowledge graphs and validating with experimental datasets to...

258 views February 18, 2025

In an era of near-limitless public experimental data but little standardization,...

QIAGEN CLC Genomics

Workflow construction and customization using QIAGEN CLC Genomics Workbench

280 views February 13, 2025

Recently we have received some requests from CLC users (as well as CLC RNA-seq...