Streamlined dPCR workflow
for lentiviral characterization and QC of cell & gene therapies
One tool to predict adverse drug reactions
Meet your new PGx powerhouse
Tips and tricks for plasmid DNA isolation success
Why diversity matters
in the human microbiome sciences
The fine art of digital PCR:
Decrypting the dMIQE guidelines and applications in applied testing
Accelerating microbiome research:
Accurate and rapid characterization of key microbial species using nanoplate digital PCR
Achieving Good Manufacturing Production (GxP)
compliance with NGS
Agilent Alissa to QCI Interpret:
How can your lab reduce the stress and complexity of transitioning to a new clinical informatics platform?
A Cost-benefit Analysis on the Use of Nylon 4N6FLOQSwabs:
Examples and Potential Benefits
Analytical considerations
for cfDNA biomarker analysis powered by NGS
Enhancing Preclinical Research Precision:
Analyzing CAR-T Biodistribution with Digital PCR (dPCR) (North & South America)
Urine cfDNA:
a new era for liquid biopsy research
Antimicrobial resistance research –
get inspired by the latest scientific talks
"Ask me anything" again:
Digital PCR edition
"Ask me anything":
The Insight Exchange on Cell Line Development
Day 1
Day 2
The epididymis:
Balancing the burden and responsibility of fertility
Beyond the Basics:
Tips and tricks to navigate plant DNA extraction
Big data meets reductionist experimentation:
A synthetic fecal transplant clarifies resistance to C. difficile infection
Can you trust AI for germline variant curation?
A Stanford University case study
Cell-free DNA variant sequencing using plasma
and AR-V7 testing of circulating tumor cells in prostate cancer patients
How to combine high-accuracy cell sorting
with multiplex digital PCR for single cell analysis
Analytical considerations for cfDNA biomarker analysis
powered by NGS
Characterization of gene expression changes
in host and microbiome interactions
What’s new
in QIAGEN CLC Genomics Workbench version 24
How to accelerate your clinical reporting workflow
for high-throughput oncology NGS testing
A breakthrough for rare disease:
Completing the Clinical exome gap!
Comprehensive Molecular Tumor Analysis (CMTA)
integrating RNAseq and tumor immune microenvironment (TME) for targeted therapy
Introducing a consolidated workflow
for DNA and RNA library preparation from a single sample
Part 2: Decoding long-reads with powerful bioinformatics tools
Differential impact of PD-1
or TIGIT genetic deletion in melanoma-specific CD8+ T cells
Digital PCR in oncohematology
Digital PCR:
make every molecule count
Comparison and analytical bridging of digital PCR platforms
for AAV titration
Discovery of immunogenic neo-peptides
from actionable RNA fusions for developing cancer vaccines
Automated DNA recovery
and typing from fired cartridge casings and firearms
In pursuit of pathogens:
Using dPCR and sequencing for microbial surveillance
Development of dPCR-based molecular MRD
for acute myeloid leukemia
Two case studies:
Digital PCR in RNA editing and testing of drug safety
EHEC Testing Redefined:
Unveiling a Major Breakthrough
Evaluation of the QIAcuity digital PCR system
for the quantitative detection of BK and JC polyomaviruses
Exome experts:
Improving the interpretation and integration of exome testing in routine clinical care
Exploring the use of dPCR for viral infections
Fast molecular subtyping of gliomas
with multiplex digital PCR
Striking gold:
Finding ultra-rare variants in liquid biopsy samples using targeted NGS
ForenSeq Kintelligence Kit:
Past, Present and Future
Functional interrogation of cancer cell states in solid tumors
Get the most of microbiome data:
Depleting host DNA in tissue, swab and bodily fluid samples for deeper sequencing and better bioinformatics
Harnessing whole-blood miRNAs
and Small RNAs for cancer diagnostics
From saliva collection to virus testing:
How can sample handling impact outcomes?
How to choose the right partner
for bulk and custom manufacturing with QIAGEN Strategic Partnerships
How to improve your existing pipeline
for somatic mutation analysis, interpretation and reporting: Part 1
for somatic mutation analysis, interpretation and reporting: Part 2
How to scale-up comprehensive genomic profiling
and deliver confident variant interpretations with QCI Interpret for Oncology
How to translate complex genomic data
to clinically-oriented personalized cancer care: a real-world experience
Improving sample and library QC
in NGS core facilities
Clinician’s Roundtable:
Interpreting genomic test results for precision oncology
Lettuce Romaine Calm:
Sequencing Foodborne Pathogens
Liquid biopsy multi-analytes in cancer research:
How to get started?
Microbial Allies:
promoting crop security via agricultural microbiome manipulation
How to set up your microRNA sequencing project for success
Minimizing bias in human microbiome research
with automated DNA/RNA isolations
Developing mRNA vaccines targeting immunogenic neoantigens
translated from chimeric RNAs for the treatment and prevention of cancer
Multiplex analysis of Copy Number Variation
in liquid biopsy using dPCR: preliminary data from patients with solid tumors
Multiplex dPCR solutions
for next-generation CAR-T products
Nanoplate digital PCR for food quality and safety testing:
adulteration and allergen detection
Navigating genomic complexities
with long-read sequencing in cancer research
How decentralized and small labs can adopt high-throughput NGS analysis
with limited time and resource investment
Minimizing Bias in Microbiome Research
Accurate NGS library quantification
using nanoplate digital PCR
Next-generation metagenomics of the human microbiome:
from bench to bedside
Oligos for commercial and bulk supply
cooperation with QIAGEN Strategic Partnerships & OEM
One tool to help biopharma accelerate cancer drug discovery and repurposing:
A translational research use-case and discussion
Overcoming challenges of NGS panel workflows
for myeloid neoplasms
How to capture low-level virus-cell interactions
with Protein Interaction Coupling (PICO) technology
Part 1: AI-Powered Hereditary Disease Diagnostics:
Closing the Gap in Clinical Exome Completeness
Part 2: AI-Powered Hereditary Disease Diagnostics:
The best way to quantify phytoplasmas in plants
Ride the QIAwave for more efficient QIAcube workflows
Expert Webinar
Accelerate RNA biomarker research using our easy online portal
Scale your comprehensive genomic profiling workflow
with superior automated variant interpretation
Shed light on inherited mutations
and solve hereditary investigations with QCI Interpret
Culture-independent detection and confirmation
of Shiga-toxin-producing E. coli with next-day reporting
Simplify your PCR analysis
with automated gel electrophoresis
Standardized viral vector processing and quantification
using digital PCR
Streamline your hereditary diseases interpretation workflow
with QCI Interpret
Supercharge your AI in drug discovery
with high-quality biomedical data
Supporting antimicrobial resistance research for known and future threats
QIAGEN scientists share their expertise
Take your genome research to the next level
with QCI Interpret Translational
TB and silicosis in miners
challenges and opportunities
Molecular characterization of T-cells
and the gut microbiome diversity and function
The great dPCR debate:
Hot takes with live Q&A
Tips and tricks for faster RNA sequencing
Tips & tricks for plasmid DNA isolation
Tips and tricks to standardize your PCR
Tips & tricks for targeted sequencing panel design
Part 1: Overcoming hurdles for molecular assay manufacturers using RT-qPCR
Part 2: Toolboxes to commercialize your molecular assay:
Taq Polymerases and Reverse Transcriptases
Uncover molecular drivers
of the tumor microenvironment using curated data and predictive modeling
Unlocking Insights with QIAGEN IPA:
Compare, Match, and Visualize Publicly Curated Datasets Alongside Your Research
From discovery to verification:
Unlocking miRNA biomarkers with NGS and digital PCR
Using COSMIC to predict, identify, and avoid mutational consequences
of cancer therapies during early drug development and in patients
Viral vector integrity analysis
Advancements in gene therapy development
in QIAGEN CLC Genomics Workbench version 23