
Explore lab automation for high-throughput discovery science in undergraduate and graduate courses. Learn about integrating research-scale automation, designing scripts, and embracing new challenges with liquid handlers.

Explore fluorescence microscopy techniques for cancer research, covering cell staining, imaging methods, and applications in drug discovery and mechanism studies for 2D and 3D models.

Explore SLC25A46's role as a novel mitochondrial regulator and biomarker in breast cancer, focusing on its impact in triple-negative breast cancer and potential for targeted treatments.

Streamline somatic NGS analysis and reduce literature review time by 90% with the Human Somatic Mutation Database. Explore genomic content, clinical trials, and expert-curated insights for solid tumors and hematological malignancies.

Explore rapid next-generation sequencing innovations for faster, flexible DNA analysis in research and clinical applications, reducing turnaround time and improving cost-effectiveness.

Explore CRISPR-based technologies for detecting and destroying viral RNA, including point-of-care and massively multiplexed nucleic acid detection methods like HUDSON, SHINE, and CARMEN.

Explore CRISPR-based microfluidic biosensing for molecular diagnostics. Learn about innovative point-of-care detection methods for pathogens and cancers, combining CRISPR and microfluidic technologies.

Explore CRISPR/Cas-enabled paper microfluidics for rapid pathogen detection, including SARS-CoV-2 diagnosis and wastewater surveillance. Learn about low-cost, deployable biosensors for public health applications.

Explore CRISPR base and prime editing technologies, their applications, and potential for treating genetic disorders without harmful double-strand breaks. Learn from expert Dr. Cihan Tastan in this cutting-edge webinar.

Explore advanced structural variant detection using Sniffles2, a powerful tool for identifying complex genomic alterations with increased accuracy, speed, and functionality in long-read sequencing data.

Explore metabolic barriers to tumor immunity in pancreatic cancer, focusing on nutrient stress impact and potential strategies to enhance immunotherapy effectiveness.

Explore T cell response generation in immunosuppressive tumor environments, focusing on overcoming challenges in pancreatic cancer and enhancing dendritic cell function for effective immunotherapy.

Explore gene regulatory networks and individual-specific disruptions, focusing on disease-associated genetic variants and their impact on transcription factor binding and gene expression.

Explore high-throughput qPCR microfluidics technology for plant and animal genomics, offering singleplex accuracy, massive parallelization, and efficient screening of multiple pathogens or SNPs.

Explore strategies to minimize off-target edits in gene editing experiments. Learn best practices, considerations for different scenarios, and optimized workflows to enhance precision in genome manipulation.

Enhance microbial detection in human microbiome samples through unbiased host DNA/RNA depletion. Learn about CRISPRclean technology for improved taxonomic resolution and increased microbial genome coverage.

Explore new methods and technologies accelerating sequence-based screening of plasmids for discovery, research, and biotechnology. Learn about ExpressPlex technology and its integration with rolling-circle amplification in OCTOPUS v3.0.

Explore a comprehensive gene-to-protein workflow solution for reliable recombinant protein expression in eukaryotic cells, optimizing yields for structural and functional analyses in biomedical research and drug development.

Explore a novel integrated workflow for efficient CTC enrichment, enumeration, and identification in metastasis research. Learn about unbiased size selection and compatibility with various molecular and cellular applications.

Explore a comprehensive structural variation map of Han Chinese genomes using long-read sequencing, uncovering genetic insights and implications for human evolution and disease.

Explore genome sequencing, from genotype to phenotype, with a focus on telomere length and its implications for aging, disease, and health disparities in minority populations.